midodrine has been researched along with Symptom Cluster in 6 studies
Midodrine: An ethanolamine derivative that is an adrenergic alpha-1 agonist. It is used as a vasoconstrictor agent in the treatment of HYPOTENSION.
midodrine : An aromatic ether that is 1,4-dimethoxybenzene which is substituted at position 2 by a 2-(glycylamino)-1-hydroxyethyl group. A direct-acting sympathomimetic with selective alpha-adrenergic agonist activity, it is used (generally as its hydrochloride salt) as a peripheral vasoconstrictor in the treatment of certain hypotensive states. The main active moiety is its major metabolite, deglymidodrine.
Excerpt | Relevance | Reference |
---|---|---|
"We assessed the potency of octreotide and midodrine, and their combination, in the treatment of the postural tachycardia syndrome (POTS) and orthostatic intolerance (OI)." | 9.12 | Treatment of postural tachycardia syndrome: a comparison of octreotide and midodrine. ( Bryner, KD; Hobbs, G; Hoeldtke, ME; Hoeldtke, RD, 2006) |
"We assessed the potency of octreotide and midodrine, and their combination, in the treatment of the postural tachycardia syndrome (POTS) and orthostatic intolerance (OI)." | 5.12 | Treatment of postural tachycardia syndrome: a comparison of octreotide and midodrine. ( Bryner, KD; Hobbs, G; Hoeldtke, ME; Hoeldtke, RD, 2006) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (16.67) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 4 (66.67) | 29.6817 |
2010's | 1 (16.67) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Noyes, AM | 1 |
Kluger, J | 1 |
Honma, K | 1 |
Hoeldtke, RD | 1 |
Bryner, KD | 1 |
Hoeldtke, ME | 1 |
Hobbs, G | 1 |
Gordon, VM | 1 |
Opfer-Gehrking, TL | 1 |
Novak, V | 1 |
Low, PA | 1 |
Samniah, N | 1 |
Iskos, D | 1 |
Sakaguchi, S | 1 |
Lurie, KG | 1 |
Benditt, DG | 1 |
Sütsch, G | 1 |
Vetter, W | 1 |
Hess, OM | 1 |
Rhyner, K | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
A Double-Blinded, Placebo-Controlled Study To Assess Hemodynamic Changes, Orthostatic Tolerance, Out-Patient Fatigue And Quality Of Life In Neuropathic And Non-Neuropathic POTS Patients In Response To Adrenoreceptor Agonist And Antagonist[NCT03070730] | Phase 1/Phase 2 | 8 participants (Actual) | Interventional | 2011-08-15 | Terminated (stopped due to Recruitment was slow and subjects declined participation after signing the ICF.) | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
(NCT03070730)
Timeframe: 1 week after first intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
(NCT03070730)
Timeframe: 1 week after second intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
(NCT03070730)
Timeframe: 1 week after third intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
A 14 item self-report questionnaire. Subjects respond on a continuum of 1 to 4 questions evaluating fatigue intensity while distinguishing physical from mental fatigue. (NCT03070730)
Timeframe: 2 weeks after first intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
A 14 item self-report questionnaire. Subjects respond on a continuum of 1 to 4 questions evaluating fatigue intensity while distinguishing physical from mental fatigue. (NCT03070730)
Timeframe: 2 weeks after second intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
A 14 item self-report questionnaire. Subjects respond on a continuum of 1 to 4 questions evaluating fatigue intensity while distinguishing physical from mental fatigue. (NCT03070730)
Timeframe: up to 3 days after randomization
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
(NCT03070730)
Timeframe: 1 week after first intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
(NCT03070730)
Timeframe: 1 week after second intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
(NCT03070730)
Timeframe: 1 week after third intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
Maximal postural tachycardia is the maximum heart rate during a 20-min tilt table test. (NCT03070730)
Timeframe: Up to 3 days after randomization
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
(NCT03070730)
Timeframe: 1 week after first intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
(NCT03070730)
Timeframe: 1 week after second intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
(NCT03070730)
Timeframe: 1 week after third intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
"Measures of follow up testing will be the scores on the physical functioning subscale of the 7 item patient global impression of change with items anchored by :very much better to very much worse." (NCT03070730)
Timeframe: 1 week after first intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
"Measures of follow up testing will be the scores on the physical functioning subscale of the 7 item patient global impression of change with items anchored by :very much better to very much worse." (NCT03070730)
Timeframe: 1 week after second intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
"Measures of follow up testing will be the scores on the physical functioning subscale of the 7 item patient global impression of change with items anchored by :very much better to very much worse." (NCT03070730)
Timeframe: 1 week after third intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
Measures of follow up testing will be the scores on the physical functioning subscale of the Hospital Anxiety and Depression Scales. (NCT03070730)
Timeframe: 1 week after first intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
Measures of follow up testing will be the scores on the physical functioning subscale of the Hospital Anxiety and Depression Scales. (NCT03070730)
Timeframe: 1 week after second intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
Measures of follow up testing will be the scores on the physical functioning subscale of the Hospital Anxiety and Depression Scales. (NCT03070730)
Timeframe: 1 week after third intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
Measures of follow up testing will be the scores on the physical functioning subscale of the Checklist Individual Strength (CIS). (NCT03070730)
Timeframe: 1 week after first intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
Measures of follow up testing will be the scores on the physical functioning subscale of the Checklist Individual Strength (CIS). (NCT03070730)
Timeframe: 1 week after second intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
Measures of follow up testing will be the scores on the physical functioning subscale of the Checklist Individual Strength (CIS). (NCT03070730)
Timeframe: 1 week after third intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
Measures of follow up testing will be the scores on the physical functioning subscale of the EuroQOL. (NCT03070730)
Timeframe: 1 week after first intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
Measures of follow up testing will be the scores on the physical functioning subscale of the EuroQOL. (NCT03070730)
Timeframe: 1 week after second intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
Measures of follow up testing will be the scores on the physical functioning subscale of the EuroQOL. (NCT03070730)
Timeframe: 1 week after third intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
Measures of follow up testing will be the scores on the physical functioning subscale of the Fatigue Severity Scale. (NCT03070730)
Timeframe: 1 week after first intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
Measures of follow up testing will be the scores on the physical functioning subscale of the Fatigue Severity Scale. (NCT03070730)
Timeframe: 1 week after second intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
Measures of follow up testing will be the scores on the physical functioning subscale of the Fatigue Severity Scale. (NCT03070730)
Timeframe: 1 week after third intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
Measures of follow up testing will be the scores on the physical functioning subscale of the Multidimensional Fatigue Inventory (MFI). (NCT03070730)
Timeframe: 1 week after first intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
Measures of follow up testing will be the scores on the physical functioning subscale of the Multidimensional Fatigue Inventory (MFI). (NCT03070730)
Timeframe: 1 week after second intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
Measures of follow up testing will be the scores on the physical functioning subscale of the Multidimensional Fatigue Inventory (MFI). (NCT03070730)
Timeframe: 1 week after third intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
Measures of follow up testing will be the scores on the physical functioning subscale of the Orthostatic Intolerance Questionnaire. (NCT03070730)
Timeframe: 1 week after first intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
Measures of follow up testing will be the scores on the physical functioning subscale of the Orthostatic Intolerance Questionnaire. (NCT03070730)
Timeframe: 1 week after second intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
Measures of follow up testing will be the scores on the physical functioning subscale of the Orthostatic Intolerance Questionnaire. (NCT03070730)
Timeframe: 1 week after third intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
Measures of follow up testing will be the scores on the physical functioning subscale of the SF-36 questionnaire. (NCT03070730)
Timeframe: 1 week after first intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
Measures of follow up testing will be the scores on the physical functioning subscale of the SF-36 questionnaire. (NCT03070730)
Timeframe: 1 week after second intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
Measures of follow up testing will be the scores on the physical functioning subscale of the SF-36 questionnaire. (NCT03070730)
Timeframe: 1 week after third intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
(NCT03070730)
Timeframe: 1 week after first intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
(NCT03070730)
Timeframe: 1 week after second intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
(NCT03070730)
Timeframe: 1 week after third intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
Maximal postural tachycardia is the maximum heart rate during a 20-min tilt table test. (NCT03070730)
Timeframe: 2 weeks after first intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
Maximal postural tachycardia is the maximum heart rate during a 20-min tilt table test. (NCT03070730)
Timeframe: 2 weeks after second intervention
Intervention | () |
---|---|
Atenolol | 0 |
Placebos | 0 |
Droxidopa | 0 |
1 review available for midodrine and Symptom Cluster
Article | Year |
---|---|
[Diabetes mellitus and orthostatic intolerance].
Topics: Bandages; Diabetic Neuropathies; Diet, Sodium-Restricted; Exercise Therapy; Heart Rate; Humans; Male | 2005 |
1 trial available for midodrine and Symptom Cluster
Article | Year |
---|---|
Treatment of postural tachycardia syndrome: a comparison of octreotide and midodrine.
Topics: Adult; Blood Pressure; Data Interpretation, Statistical; Dizziness; Drug Therapy, Combination; Femal | 2006 |
4 other studies available for midodrine and Symptom Cluster
Article | Year |
---|---|
A tale of two syndromes: Lyme disease preceding postural orthostatic tachycardia syndrome.
Topics: Adolescent; Adult; Anti-Arrhythmia Agents; Diet, Gluten-Free; Female; Fluid Therapy; Humans; Lyme Di | 2015 |
Hemodynamic and symptomatic effects of acute interventions on tilt in patients with postural tachycardia syndrome.
Topics: Adolescent; Adult; Anti-Arrhythmia Agents; Antihypertensive Agents; Clonidine; Female; Hemodynamics; | 2000 |
Syncope in pharmacologically unmasked Brugada syndrome: indication for an implantable defibrillator or an unresolved dilemma?
Topics: Adult; Bundle-Branch Block; Defibrillators, Implantable; Diagnosis, Differential; Electrocardiograph | 2001 |
[Dizziness, syncope, orthostatic hypotension].
Topics: Aged; Dizziness; Epinephrine; Female; Humans; Hypotension, Orthostatic; Midodrine; Norepinephrine; S | 1988 |