indomethacin has been researched along with Episcleritis in 15 studies
Indomethacin: A non-steroidal anti-inflammatory agent (NSAID) that inhibits CYCLOOXYGENASE, which is necessary for the formation of PROSTAGLANDINS and other AUTACOIDS. It also inhibits the motility of POLYMORPHONUCLEAR LEUKOCYTES.
indometacin : A member of the class of indole-3-acetic acids that is indole-3-acetic acid in which the indole ring is substituted at positions 1, 2 and 5 by p-chlorobenzoyl, methyl, and methoxy groups, respectively. A non-steroidal anti-inflammatory drug, it is used in the treatment of musculoskeletal and joint disorders including osteoarthritis, rheumatoid arthritis, gout, bursitis and tendinitis.
Excerpt | Relevance | Reference |
---|---|---|
"Six patients with diffuse or nodular scleritis that did not respond satisfactorily to oral indomethacin or prednisone used alone required a combination of these two drugs to achieve a complete clinical response." | 7.67 | Treatment of scleritis with combined oral prednisone and indomethacin therapy. ( Mondino, BJ; Phinney, RB, 1988) |
"Posterior scleritis is a rare disease, the clinical signs of which may vary." | 5.29 | Recognition of posterior scleritis and its treatment with indomethacin. ( Robertson, JE; Rosenbaum, JT, 1993) |
"Six patients with diffuse or nodular scleritis that did not respond satisfactorily to oral indomethacin or prednisone used alone required a combination of these two drugs to achieve a complete clinical response." | 3.67 | Treatment of scleritis with combined oral prednisone and indomethacin therapy. ( Mondino, BJ; Phinney, RB, 1988) |
"Posterior scleritis is an unusual disease that may cause serious ocular inflammation and potentially blinding consequences." | 1.34 | Isolated bilateral posterior scleritis after eye trauma. ( Ramirez-Ortiz, MA; Vasquez-Resendis, A, 2007) |
"Although scleritis has not been reported as a tubulointerstitial nephritis-associated ocular inflammation, it may be part of the possible spectrum of ocular inflammation occurring as part of the TINU syndrome." | 1.33 | Recurrent nodular scleritis preceding an adult TINU syndrome. ( Daniel, E; Gangaputra, S; Jabs, DA; Kempen, JH, 2006) |
"Posterior scleritis has protean manifestations and can be easily overlooked." | 1.32 | [Posterior scleritis: six case reports]. ( Attia, S; Bhouri, L; Chaouch, K; Jelliti, B; Jenzri, S; Khairallah, M; Ladjimi, A; Messaoud, R; Zaouali, S, 2003) |
"Scleritis is a severe ocular inflammation, often associated with ocular complications, and nearly always treated with systemic medications." | 1.31 | Episcleritis and scleritis: clinical features and treatment results. ( Dunn, JP; Jabs, DA; Marsh, MJ; Mudun, A, 2000) |
"Posterior scleritis is a rare disease, the clinical signs of which may vary." | 1.29 | Recognition of posterior scleritis and its treatment with indomethacin. ( Robertson, JE; Rosenbaum, JT, 1993) |
"Patients with colitis or ileocolitis were more likely to suffer from ocular inflammation (23." | 1.28 | Ocular inflammation in Crohn's disease. ( Murray, AD; Salmon, JF; Wright, JP, 1991) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 3 (20.00) | 18.7374 |
1990's | 4 (26.67) | 18.2507 |
2000's | 5 (33.33) | 29.6817 |
2010's | 3 (20.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Moussa, K | 1 |
Shantha, J | 1 |
Schallhorn, JM | 1 |
Takkar, B | 1 |
Khokhar, S | 1 |
Kumar, U | 1 |
Venkatesh, P | 1 |
Liu, AT | 1 |
Luk, FO | 1 |
Chan, CK | 1 |
Ladjimi, A | 1 |
Messaoud, R | 1 |
Attia, S | 1 |
Jenzri, S | 1 |
Zaouali, S | 1 |
Chaouch, K | 1 |
Bhouri, L | 1 |
Jelliti, B | 1 |
Khairallah, M | 1 |
Daniel, E | 1 |
Gangaputra, S | 1 |
Kempen, JH | 1 |
Jabs, DA | 2 |
Ramirez-Ortiz, MA | 1 |
Vasquez-Resendis, A | 1 |
Rosenbaum, JT | 1 |
Robertson, JE | 1 |
Chow, MT | 1 |
Anderson, SF | 1 |
Mudun, A | 1 |
Dunn, JP | 1 |
Marsh, MJ | 1 |
Grapă, C | 1 |
Salmon, JF | 2 |
Wright, JP | 1 |
Murray, AD | 2 |
Strauss, PC | 1 |
Todd, G | 1 |
Lightman, S | 1 |
Watson, P | 1 |
Mondino, BJ | 1 |
Phinney, RB | 1 |
Guan, ZS | 1 |
Zhong, GQ | 1 |
Hu, ZK | 1 |
Wu, ZY | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
An Open Label, Multi-centered, Randomized Phase 2 Study to Evaluate the Safety, Tolerability and Bioactivity of Subcutaneous ACTH GeL in PAtients With Scleritis: The ATLAS Study[NCT03465111] | Phase 2 | 30 participants (Anticipated) | Interventional | 2019-01-01 | Recruiting | ||
Gevokizumab Treatment for Active Scleritis By IL-1 Inhibition (GATSBY)[NCT01835132] | Phase 1/Phase 2 | 8 participants (Actual) | Interventional | 2013-03-31 | Completed | ||
A Phase I/II Study to Investigate Subconjunctival Sirolimus for the Treatment of Active Autoimmune Non-Necrotizing Anterior Scleritis[NCT01517074] | Phase 1/Phase 2 | 5 participants (Actual) | Interventional | 2012-01-31 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
Intraocular pressure (IOP) is measured in millimeters of mercury (mmHg). (NCT01835132)
Timeframe: Baseline and Final Visit
Intervention | mmHg (Mean) |
---|---|
Gevokizumab | 1.33 |
Intraocular pressure (IOP) is measured in millimeters of mercury (mmHg). (NCT01835132)
Timeframe: Baseline and Week 12
Intervention | mmHg (Mean) |
---|---|
Gevokizumab | 1.00 |
Intraocular pressure (IOP) is measured in millimeters of mercury (mmHg). (NCT01835132)
Timeframe: Baseline and Week 16
Intervention | mmHg (Mean) |
---|---|
Gevokizumab | 1.56 |
Intraocular pressure (IOP) is measured in millimeters of mercury (mmHg). (NCT01835132)
Timeframe: Baseline and Week 2
Intervention | mmHg (Mean) |
---|---|
Gevokizumab | 0.67 |
Intraocular pressure (IOP) is measured in millimeters of mercury (mmHg). (NCT01835132)
Timeframe: Baseline and Week 20
Intervention | mmHg (Mean) |
---|---|
Gevokizumab | 1.33 |
Mean Change in Intraocular pressure (IOP) is measured and reported as change in IOP between baseline and 24 weeks in millimeters of mercury (mmHg). (NCT01835132)
Timeframe: Baseline and Week 24
Intervention | mmHg (Mean) |
---|---|
Gevokizumab | 0.78 |
Intraocular pressure (IOP) is measured in millimeters of mercury (mmHg). (NCT01835132)
Timeframe: Baseline and Week 28
Intervention | mmHg (Mean) |
---|---|
Gevokizumab | 1.11 |
Intraocular pressure (IOP) is measured in millimeters of mercury (mmHg). (NCT01835132)
Timeframe: Baseline and Week 32
Intervention | mmHg (Mean) |
---|---|
Gevokizumab | 2.67 |
Intraocular pressure (IOP) is measured in millimeters of mercury (mmHg). (NCT01835132)
Timeframe: Baseline and Week 36
Intervention | mmHg (Mean) |
---|---|
Gevokizumab | 2.17 |
Intraocular pressure (IOP) is measured in millimeters of mercury (mmHg). (NCT01835132)
Timeframe: Baseline and Week 4
Intervention | mmHg (Mean) |
---|---|
Gevokizumab | 0.67 |
Intraocular pressure (IOP) is measured in millimeters of mercury (mmHg). (NCT01835132)
Timeframe: Baseline and Week 40
Intervention | mmHg (Mean) |
---|---|
Gevokizumab | 0.50 |
Intraocular pressure (IOP) is measured in millimeters of mercury (mmHg). (NCT01835132)
Timeframe: Baseline and Week 52
Intervention | mmHg (Mean) |
---|---|
Gevokizumab | 1.83 |
"This visit represents the beginning of the as-needed 2nd Extension Phase at Week 52. If eligible, participants continued with injections at Wks 52, 54, 58 and 62.~Intraocular pressure (IOP) is measured in millimeters of mercury (mmHg)." (NCT01835132)
Timeframe: Baseline and Week 52A
Intervention | mmHg (Mean) |
---|---|
Gevokizumab | -0.67 |
Intraocular pressure (IOP) is measured in millimeters of mercury (mmHg). (NCT01835132)
Timeframe: Baseline and Week 54
Intervention | mmHg (Mean) |
---|---|
Gevokizumab | 1.33 |
Intraocular pressure (IOP) is measured in millimeters of mercury (mmHg). (NCT01835132)
Timeframe: Baseline and Week 58
Intervention | mmHg (Mean) |
---|---|
Gevokizumab | 1.33 |
Intraocular pressure (IOP) is measured in millimeters of mercury (mmHg). (NCT01835132)
Timeframe: Baseline and Week 62
Intervention | mmHg (Mean) |
---|---|
Gevokizumab | 0.67 |
Intraocular pressure (IOP) is measured in millimeters of mercury (mmHg). (NCT01835132)
Timeframe: Baseline and Week 8
Intervention | mmHg (Mean) |
---|---|
Gevokizumab | 1.11 |
Visual acuity was measured using the Early Treatment Diabetic Retinopathy Study (ETDRS) protocol. Acuity is measured as letters read on an ETDRS eye chart and the letters read equate to Snellen measurements. For example, if a participant reads between 84 and 88 letters, the equivalent Snellen measurement is 20/20. (NCT01835132)
Timeframe: Baseline and Final Visit
Intervention | ETDRS letters (Mean) |
---|---|
Gevokizumab | -2.00 |
Visual acuity was measured using the Early Treatment Diabetic Retinopathy Study (ETDRS) protocol. Acuity is measured as letters read on an ETDRS eye chart and the letters read equate to Snellen measurements. For example, if a participant reads between 84 and 88 letters, the equivalent Snellen measurement is 20/20. (NCT01835132)
Timeframe: Baseline and Week 12
Intervention | ETDRS letters (Mean) |
---|---|
Gevokizumab | 0.11 |
Visual acuity was measured using the Early Treatment Diabetic Retinopathy Study (ETDRS) protocol. Acuity is measured as letters read on an ETDRS eye chart and the letters read equate to Snellen measurements. For example, if a participant reads between 84 and 88 letters, the equivalent Snellen measurement is 20/20. (NCT01835132)
Timeframe: Baseline and Week 16
Intervention | ETDRS letters (Mean) |
---|---|
Gevokizumab | 1.00 |
Visual acuity was measured using the Early Treatment Diabetic Retinopathy Study (ETDRS) protocol. Acuity is measured as letters read on an ETDRS eye chart and the letters read equate to Snellen measurements. For example, if a participant reads between 84 and 88 letters, the equivalent Snellen measurement is 20/20. (NCT01835132)
Timeframe: Baseline and Week 2
Intervention | ETDRS letters (Mean) |
---|---|
Gevokizumab | -1.00 |
Visual acuity was measured using the Early Treatment Diabetic Retinopathy Study (ETDRS) protocol. Acuity is measured as letters read on an ETDRS eye chart and the letters read equate to Snellen measurements. For example, if a participant reads between 84 and 88 letters, the equivalent Snellen measurement is 20/20. (NCT01835132)
Timeframe: Baseline and Week 20
Intervention | ETDRS letters (Mean) |
---|---|
Gevokizumab | 1.33 |
Visual acuity was measured using the Early Treatment Diabetic Retinopathy Study (ETDRS) protocol. Acuity is measured as letters read on an ETDRS eye chart and the letters read equate to Snellen measurements. For example, if a participant reads between 84 and 88 letters, the equivalent Snellen measurement is 20/20. (NCT01835132)
Timeframe: Baseline and Week 24
Intervention | ETDRS letters (Mean) |
---|---|
Gevokizumab | -0.67 |
Visual acuity was measured using the Early Treatment Diabetic Retinopathy Study (ETDRS) protocol. Acuity is measured as letters read on an ETDRS eye chart and the letters read equate to Snellen measurements. For example, if a participant reads between 84 and 88 letters, the equivalent Snellen measurement is 20/20. (NCT01835132)
Timeframe: Baseline and Week 28
Intervention | ETDRS letters (Mean) |
---|---|
Gevokizumab | 1.00 |
Visual acuity was measured using the Early Treatment Diabetic Retinopathy Study (ETDRS) protocol. Acuity is measured as letters read on an ETDRS eye chart and the letters read equate to Snellen measurements. For example, if a participant reads between 84 and 88 letters, the equivalent Snellen measurement is 20/20. (NCT01835132)
Timeframe: Baseline and Week 32
Intervention | ETDRS letters (Mean) |
---|---|
Gevokizumab | 3.00 |
Visual acuity was measured using the Early Treatment Diabetic Retinopathy Study (ETDRS) protocol. Acuity is measured as letters read on an ETDRS eye chart and the letters read equate to Snellen measurements. For example, if a participant reads between 84 and 88 letters, the equivalent Snellen measurement is 20/20. (NCT01835132)
Timeframe: Baseline and Week 36
Intervention | ETDRS letters (Mean) |
---|---|
Gevokizumab | 1.83 |
Visual acuity was measured using the Early Treatment Diabetic Retinopathy Study (ETDRS) protocol. Acuity is measured as letters read on an ETDRS eye chart and the letters read equate to Snellen measurements. For example, if a participant reads between 84 and 88 letters, the equivalent Snellen measurement is 20/20. (NCT01835132)
Timeframe: Baseline and Week 4
Intervention | ETDRS letters (Mean) |
---|---|
Gevokizumab | -1.78 |
Visual acuity was measured using the Early Treatment Diabetic Retinopathy Study (ETDRS) protocol. Acuity is measured as letters read on an ETDRS eye chart and the letters read equate to Snellen measurements. For example, if a participant reads between 84 and 88 letters, the equivalent Snellen measurement is 20/20. (NCT01835132)
Timeframe: Baseline and Week 40
Intervention | ETDRS letters (Mean) |
---|---|
Gevokizumab | 2.67 |
Visual acuity was measured using the Early Treatment Diabetic Retinopathy Study (ETDRS) protocol. Acuity is measured as letters read on an ETDRS eye chart and the letters read equate to Snellen measurements. For example, if a participant reads between 84 and 88 letters, the equivalent Snellen measurement is 20/20. (NCT01835132)
Timeframe: Baseline and Week 52
Intervention | ETDRS letters (Mean) |
---|---|
Gevokizumab | 0.17 |
"This visit represents the beginning of the as-needed 2nd Extension Phase at Week 52. If eligible, participants continued with injections at Wks 52, 54, 58 and 62.~Visual acuity was measured using the Early Treatment Diabetic Retinopathy Study (ETDRS) protocol. Acuity is measured as letters read on an ETDRS eye chart and the letters read equate to Snellen measurements. For example, if a participant reads between 84 and 88 letters, the equivalent Snellen measurement is 20/20." (NCT01835132)
Timeframe: Baseline and Week 52A
Intervention | ETDRS letters (Mean) |
---|---|
Gevokizumab | -8.00 |
Visual acuity was measured using the Early Treatment Diabetic Retinopathy Study (ETDRS) protocol. Acuity is measured as letters read on an ETDRS eye chart and the letters read equate to Snellen measurements. For example, if a participant reads between 84 and 88 letters, the equivalent Snellen measurement is 20/20. (NCT01835132)
Timeframe: Baseline and Week 54
Intervention | ETDRS letters (Mean) |
---|---|
Gevokizumab | -0.67 |
Visual acuity was measured using the Early Treatment Diabetic Retinopathy Study (ETDRS) protocol. Acuity is measured as letters read on an ETDRS eye chart and the letters read equate to Snellen measurements. For example, if a participant reads between 84 and 88 letters, the equivalent Snellen measurement is 20/20. (NCT01835132)
Timeframe: Baseline and Week 58
Intervention | ETDRS letters (Mean) |
---|---|
Gevokizumab | -1.33 |
Visual acuity was measured using the Early Treatment Diabetic Retinopathy Study (ETDRS) protocol. Acuity is measured as letters read on an ETDRS eye chart and the letters read equate to Snellen measurements. For example, if a participant reads between 84 and 88 letters, the equivalent Snellen measurement is 20/20. (NCT01835132)
Timeframe: Baseline and Week 62
Intervention | ETDRS letters (Mean) |
---|---|
Gevokizumab | -1.33 |
Visual acuity was measured using the Early Treatment Diabetic Retinopathy Study (ETDRS) protocol. Acuity is measured as letters read on an ETDRS eye chart and the letters read equate to Snellen measurements. For example, if a participant reads between 84 and 88 letters, the equivalent Snellen measurement is 20/20. (NCT01835132)
Timeframe: Baseline and Week 8
Intervention | ETDRS letters (Mean) |
---|---|
Gevokizumab | 0.78 |
Scleral inflammation was graded following 10% Phenylephrine application with an ordinal scale of 0 (no scleral inflammation with complete blanching of vessels), 0.5+ (minimal/trace inflammation with localized pink appearance of the sclera around minimally dilated deep episcleral vessels), 1+ (mild inflammation with diffuse pink appearance of the sclera around mildly dilated deep episcleral vessels), 2+ (moderate inflammation with purplish pink appearance of the sclera with tortuous and engorged deep episcleral vessels), 3+ (severe inflammation with diffuse significant redness of sclera, the details of superficial and deep episcleral vessels can't be observed), and 4+ (necrotizing inflammation with diffuse redness of the sclera with scleral thinning and uveal show). (NCT01835132)
Timeframe: Baseline and Week 16
Intervention | participants (Number) |
---|---|
Gevokizumab | 6 |
Visual acuity was measured using the Early Treatment Diabetic Retinopathy Study (ETDRS) protocol. Acuity is measured as letters read on an ETDRS eye chart and the letters read equate to Snellen measurements. For example, if a participant reads between 84 and 88 letters, the equivalent Snellen measurement is 20/20. (NCT01835132)
Timeframe: Post-injection through study completion, up to 78 weeks per participant
Intervention | participants (Number) |
---|---|
Gevokizumab | 0 |
Visual acuity was measured using the Early Treatment Diabetic Retinopathy Study (ETDRS) protocol. Acuity is measured as letters read on an ETDRS eye chart and the letters read equate to Snellen measurements. For example, if a participant reads between 84 and 88 letters, the equivalent Snellen measurement is 20/20. (NCT01517074)
Timeframe: Baseline and Week 52
Intervention | letters read (Mean) |
---|---|
Study Eye | -0.25 |
Fellow Eye | -2.25 |
For participants who demonstrate active inflammation (incomplete or no response to initial injection) or experience a flare-up (as defined by a ≥1-step increase in scleral inflammation) after the initial injection (NCT01517074)
Timeframe: Baseline and Week 52
Intervention | Days (Mean) |
---|---|
Sirolimus | 65.3 |
Visual acuity was measured using the Early Treatment Diabetic Retinopathy Study (ETDRS) protocol. Acuity is measured as letters read on an ETDRS eye chart and the letters read equate to Snellen measurements. For example, if a participant reads between 84 and 88 letters, the equivalent Snellen measurement is 20/20. (NCT01517074)
Timeframe: Baseline and Week 52
Intervention | letters read (Median) |
---|---|
Study Eye | 0.00 |
Fellow Eye | -2.50 |
Participants that still demonstrate active inflammation (incomplete or no response to initial injection) or experience a flare-up (as defined by a ≥1-step increase in scleral inflammation) after the initial injection will be eligible for a re-injection in the study eye at or after Week 4 (not to exceed a dose of 1,320 μg per eye within an eight-week period). (NCT01517074)
Timeframe: Baseline and Week 52
Intervention | participants (Number) |
---|---|
Sirolimus | 3 |
Scleral inflammation was graded following 10% Phenylephrine application with an ordinal scale of 0 (no scleral inflammation with complete blanching of vessels), 0.5+ (minimal/trace inflammation with localized pink appearance of the sclera around minimally dilated deep episcleral vessels), 1+ (mild inflammation with diffuse pink appearance of the sclera around mildly dilated deep episcleral vessels), 2+ (moderate inflammation with purplish pink appearance of the sclera with tortuous and engorged deep episcleral vessels), 3+ (severe inflammation with diffuse significant redness of sclera, the details of superficial and deep episcleral vessels can't be observed), and 4+ (necrotizing inflammation with diffuse redness of the sclera with scleral thinning and uveal show) (NCT01517074)
Timeframe: Baseline and Week 52
Intervention | participants (Number) |
---|---|
Sirolimus | 3 |
A substantial rise in intraocular pressure can be defined as ≥10 mmHg change in pressure. (NCT01517074)
Timeframe: Baseline and Week 52
Intervention | participants (Number) |
---|---|
Sirolimus | 0 |
"The primary efficacy outcome was a 2-step reduction in scleritis grading out of a scale of 0 to 4+ (where 0.5+ is recognized as an ordinal step between 1+ and 0+).~Scleral inflammation was graded following 10% Phenylephrine application with an ordinal scale of 0 (no scleral inflammation with complete blanching of vessels), 0.5+ (minimal/trace inflammation with localized pink appearance of the sclera around minimally dilated deep episcleral vessels), 1+ (mild inflammation with diffuse pink appearance of the sclera around mildly dilated deep episcleral vessels), 2+ (moderate inflammation with purplish pink appearance of the sclera with tortuous and engorged deep episcleral vessels), 3+ (severe inflammation with diffuse significant redness of sclera, the details of superficial and deep episcleral vessels can't be observed), and 4+ (necrotizing inflammation with diffuse redness of the sclera with scleral thinning and uveal show)." (NCT01517074)
Timeframe: Baseline and Week 8
Intervention | participants (Number) |
---|---|
Sirolimus | 5 |
(NCT01517074)
Timeframe: Baseline and Week 52
Intervention | participants (Number) |
---|---|
Sirolimus | 2 |
(NCT01517074)
Timeframe: Baseline and Week 52
Intervention | participants (Number) |
---|---|
Sirolimus | 0 |
Four (4) out of 5 participants were on immunosuppressive medications at enrollment. (NCT01517074)
Timeframe: Week 16 and Week 52
Intervention | participants (Number) |
---|---|
Sirolimus | 1 |
Visual acuity was measured using the Early Treatment Diabetic Retinopathy Study (ETDRS) protocol. Acuity is measured as letters read on an ETDRS eye chart and the letters read equate to Snellen measurements. For example, if a participant reads between 84 and 88 letters, the equivalent Snellen measurement is 20/20. (NCT01517074)
Timeframe: Baseline to Week 52
Intervention | Participants (Count of Participants) |
---|---|
Study Eye | 0 |
Fellow Eye | 1 |
Scleral inflammation was graded following 10% Phenylephrine application with an ordinal scale of 0 (no scleral inflammation with complete blanching of vessels), 0.5+ (minimal/trace inflammation with localized pink appearance of the sclera around minimally dilated deep episcleral vessels), 1+ (mild inflammation with diffuse pink appearance of the sclera around mildly dilated deep episcleral vessels), 2+ (moderate inflammation with purplish pink appearance of the sclera with tortuous and engorged deep episcleral vessels), 3+ (severe inflammation with diffuse significant redness of sclera, the details of superficial and deep episcleral vessels can't be observed), and 4+ (necrotizing inflammation with diffuse redness of the sclera with scleral thinning and uveal show) (NCT01517074)
Timeframe: Baseline and Week 52
Intervention | score on a scale (Number) | |||
---|---|---|---|---|
Participant 001 | Participant 002 | Participant 003 | Participant 005 | |
Scleral Inflammation Score at Baseline | 3 | 1 | 3 | 3 |
Scleral Inflammation Score at Week 52 | 0 | 0 | 0 | 0 |
Step Changes in Scleral Inflammation at Week 52 From Baseline | -4 | -2 | -4 | -4 |
15 other studies available for indomethacin and Episcleritis
Article | Year |
---|---|
Blurry Vision and Eye Pain After Pterygium Surgery.
Topics: Administration, Oral; Aged; Anti-Bacterial Agents; Anti-Inflammatory Agents, Non-Steroidal; Eye Infe | 2018 |
Necrotising scleritis, keratitis and uveitis in primary antiphospholipid syndrome.
Topics: Administration, Oral; Administration, Topical; Anti-Inflammatory Agents, Non-Steroidal; Antiphosphol | 2018 |
A case of giant nodular posterior scleritis mimicking choroidal malignancy.
Topics: Administration, Oral; Adult; Anti-Inflammatory Agents, Non-Steroidal; Choroid Neoplasms; Diagnosis, | 2015 |
[Posterior scleritis: six case reports].
Topics: Administration, Oral; Adolescent; Adrenal Cortex Hormones; Adult; Anti-Inflammatory Agents; Anti-Inf | 2003 |
Recurrent nodular scleritis preceding an adult TINU syndrome.
Topics: Acute Disease; Female; Glucocorticoids; Humans; Indomethacin; Middle Aged; Nephritis, Interstitial; | 2006 |
Isolated bilateral posterior scleritis after eye trauma.
Topics: Azathioprine; Child; Conjunctiva; Drug Therapy, Combination; Eye Injuries; Eyelids; Female; Fluoresc | 2007 |
Recognition of posterior scleritis and its treatment with indomethacin.
Topics: Adult; Female; Fluorescein Angiography; Follow-Up Studies; Fundus Oculi; Humans; Indomethacin; Male; | 1993 |
Relapsing polychondritis.
Topics: Aged; Aged, 80 and over; Anti-Inflammatory Agents; Anti-Inflammatory Agents, Non-Steroidal; Choroid | 2000 |
Episcleritis and scleritis: clinical features and treatment results.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Anti-Inflammatory Agents; Anti-Inflammatory Agents, Non- | 2000 |
Episcleritis and scleritis: clinical features and treatment results.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Anti-Inflammatory Agents; Anti-Inflammatory Agents, Non- | 2000 |
Episcleritis and scleritis: clinical features and treatment results.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Anti-Inflammatory Agents; Anti-Inflammatory Agents, Non- | 2000 |
Episcleritis and scleritis: clinical features and treatment results.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Anti-Inflammatory Agents; Anti-Inflammatory Agents, Non- | 2000 |
Episcleritis and scleritis: clinical features and treatment results.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Anti-Inflammatory Agents; Anti-Inflammatory Agents, Non- | 2000 |
Episcleritis and scleritis: clinical features and treatment results.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Anti-Inflammatory Agents; Anti-Inflammatory Agents, Non- | 2000 |
Episcleritis and scleritis: clinical features and treatment results.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Anti-Inflammatory Agents; Anti-Inflammatory Agents, Non- | 2000 |
Episcleritis and scleritis: clinical features and treatment results.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Anti-Inflammatory Agents; Anti-Inflammatory Agents, Non- | 2000 |
Episcleritis and scleritis: clinical features and treatment results.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Anti-Inflammatory Agents; Anti-Inflammatory Agents, Non- | 2000 |
[Palindromic posterior scleritis].
Topics: Diagnosis, Differential; Drug Therapy, Combination; Female; Humans; Hydrocortisone; Indomethacin; Mi | 1991 |
Ocular inflammation in Crohn's disease.
Topics: Adolescent; Adult; Aged; Anterior Eye Segment; Anti-Inflammatory Agents, Non-Steroidal; Child; Colit | 1991 |
Acute scleritis in porphyria cutanea tarda.
Topics: Acute Disease; Aged; Bloodletting; Female; Humans; Indomethacin; Male; Middle Aged; Porphyrias; Porp | 1990 |
Treatment of scleritis with combined oral prednisone and indomethacin therapy.
Topics: Administration, Oral; Drug Therapy, Combination; Humans; Indomethacin; Prednisone; Scleritis | 1989 |
Treatment of scleritis with combined oral prednisone and indomethacin therapy.
Topics: Administration, Oral; Drug Combinations; Female; Humans; Indomethacin; Male; Middle Aged; Prednisone | 1988 |
[Treatment of necrotising scleritis].
Topics: Adult; Aged; Combined Modality Therapy; Cyclophosphamide; Drug Therapy, Combination; Female; Humans; | 1988 |