ketorolac has been researched along with Rhinitis in 1 studies
Ketorolac: A pyrrolizine carboxylic acid derivative structurally related to INDOMETHACIN. It is an NSAID and is used principally for its analgesic activity. (From Martindale The Extra Pharmacopoeia, 31st ed)
ketorolac : A racemate comprising equimolar amounts of (R)-(+)- and (S)-(-)-5-benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid. While only the (S)-(-) enantiomer is a COX1 and COX2 inhibitor, the (R)-(+) enantiomer exhibits potent analgesic activity. A non-steroidal anti-inflammatory drug, ketorolac is mainly used (generally as the tromethamine salt) for its potent analgesic properties in the short-term management of post-operative pain, and in eye drops to relieve the ocular itching associated with seasonal allergic conjunctivitis. It was withdrawn from the market in many countries in 1993 following association with haemorrhage and renal failure.
5-benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid : A member of the class of pyrrolizines that is 2,3-dihydro-1H-pyrrolizine which is substituted at positions 1 and 5 by carboxy and benzoyl groups, respectively.
Rhinitis: Inflammation of the NASAL MUCOSA, the mucous membrane lining the NASAL CAVITIES.
Excerpt | Relevance | Reference |
---|---|---|
" Following implant surgery, postoperative pain was rated moderate or severe in 25/28 patients (89 percent), requiring prn analgesic dosing for up to 3 days in 14/25 individuals (56 percent)." | 1.39 | Characterization and treatment of postsurgical dental implant pain employing intranasal ketorolac. ( Bockow, R; Bodner, L; Hersh, EV; Hutcheson, M; Korostoff, J; Pinto, A; Secreto, SA, 2013) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Bockow, R | 1 |
Korostoff, J | 1 |
Pinto, A | 1 |
Hutcheson, M | 1 |
Secreto, SA | 1 |
Bodner, L | 1 |
Hersh, EV | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Single-dose and Multi-dose Open-label Pilot Trial of the Analgesic Efficacy and Tolerability of Intranasal Ketorolac Tromethamine (SPRIX®) in Dental Implant Surgery Patients With Postoperative Pain.[NCT01490931] | Phase 4 | 28 participants (Actual) | Interventional | 2011-11-30 | Completed | ||
Demonstration of OTC Naproxen Sodium's (Aleve's) Anti-inflammatory Action in Dental Implant Surgery Patients[NCT04694300] | Phase 4 | 32 participants (Actual) | Interventional | 2021-02-07 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
(NCT01490931)
Timeframe: 2 Hours
Intervention | millimeters (Mean) |
---|---|
Ketorolac Nasal Spray 31.5 mg (SPRIX) | 9.1 |
Pain intensity scores will be recorded by patient employing a standard 100 mm visual analog scale (NCT01490931)
Timeframe: 20 minutes post dose
Intervention | millimeters (Mean) |
---|---|
Ketorolac Nasal Spray 31.5 mg (SPRIX) | 14.3 |
(NCT01490931)
Timeframe: 3 hours post-dose
Intervention | millimeters (Mean) |
---|---|
Ketorolac Nasal Spray 31.5 mg (SPRIX) | 9.6 |
(NCT01490931)
Timeframe: 4 Hours post-dose
Intervention | millimeters (Mean) |
---|---|
Ketorolac Nasal Spray 31.5 mg (SPRIX) | 10.0 |
VAS pain intensity score at 40 minutes post-dose (NCT01490931)
Timeframe: 40 minutes post dose
Intervention | millimeters (Mean) |
---|---|
Ketorolac Nasal Spray 31.5 mg (SPRIX) | 10.1 |
(NCT01490931)
Timeframe: 5 Hours post-dose
Intervention | millimeters (Mean) |
---|---|
Ketorolac Nasal Spray 31.5 mg (SPRIX) | 16.2 |
(NCT01490931)
Timeframe: 6 Hours post-dose
Intervention | millimeters (Mean) |
---|---|
Ketorolac Nasal Spray 31.5 mg (SPRIX) | 19.8 |
VAS pain intensity score 60 minutes after dosing. (NCT01490931)
Timeframe: 60 minutes post dose
Intervention | millimeters (Mean) |
---|---|
Ketorolac Nasal Spray 31.5 mg (SPRIX) | 10.6 |
(NCT01490931)
Timeframe: 90 minutes post-dose
Intervention | millimeters (Mean) |
---|---|
Ketorolac Nasal Spray 31.5 mg (SPRIX) | 9.6 |
Measure obtained using recognized double-stop watch technique. Patient is asked to depress the second stop watch when pain relief is meaningful to them. Each patient decides what meaningful relief is for them. (NCT01490931)
Timeframe: At time of depressing meaningful relief stopwatch up to 6 hours.
Intervention | seconds (Median) |
---|---|
Ketorolac Nasal Spray 31.5 mg (SPRIX) | 172 |
Self explanatory (NCT01490931)
Timeframe: Up to 5 days
Intervention | days (Number) |
---|---|
Ketorolac Nasal Spray 31.5 mg (SPRIX) | 3 |
(NCT01490931)
Timeframe: Up to 5 hours after last suture is placed
Intervention | percentage of participants (Number) |
---|---|
Ketorolac Nasal Spray 31.5 mg (SPRIX) | 89 |
Data will be obtained employing the well-described double stop watch technique (NCT01490931)
Timeframe: Censored at 6 hours
Intervention | seconds (Median) |
---|---|
Ketorolac Nasal Spray 31.5 mg (SPRIX) | 86 |
1 other study available for ketorolac and Rhinitis
Article | Year |
---|---|
Characterization and treatment of postsurgical dental implant pain employing intranasal ketorolac.
Topics: Acetaminophen; Administration, Intranasal; Adult; Analgesia, Patient-Controlled; Analgesics, Non-Nar | 2013 |
Characterization and treatment of postsurgical dental implant pain employing intranasal ketorolac.
Topics: Acetaminophen; Administration, Intranasal; Adult; Analgesia, Patient-Controlled; Analgesics, Non-Nar | 2013 |
Characterization and treatment of postsurgical dental implant pain employing intranasal ketorolac.
Topics: Acetaminophen; Administration, Intranasal; Adult; Analgesia, Patient-Controlled; Analgesics, Non-Nar | 2013 |
Characterization and treatment of postsurgical dental implant pain employing intranasal ketorolac.
Topics: Acetaminophen; Administration, Intranasal; Adult; Analgesia, Patient-Controlled; Analgesics, Non-Nar | 2013 |