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Midodrine on Orthostatic Hypotension in Patients After Bariatric Surgery

The Effect of Midodrine on Orthostatic Hypotension in Patients After Bariatric Surgery:A Clinical Trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250825066986N1
Enrollment
90
Registered
2025-11-15
Start date
2024-12-20
Completion date
Unknown
Last updated
2025-12-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Orthostatic Hypotension post Bariatric Surgery. Other intraoperative and postprocedural complications and disorders of the circulatory system, not elsewhere classified

Interventions

Intervention 1: Intervention group: Patients will receive midodrine 2.5 mg three times daily, in addition to therapeutic recommendations including increased fluid and salt intake, use of compression s

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Age 18–65 years Underwent bariatric surgery (e.g., sleeve gastrectomy, gastric bypass, etc.) at least 4 weeks prior to study enrollment and up to 5 years post-surgery Diagnosis of orthostatic hypotension (OH) according to the following criteria:=20 mmHg drop in systolic blood pressure or =10 mmHg drop in diastolic blood pressure within 3 minutes of standing No use of midodrine or similar medications in the past 2 weeks No severe cardiovascular diseases that, according to physician assessment, contraindicate the use of midodrine

Exclusion criteria

Exclusion criteria: Intolerance to midodrine or occurrence of severe adverse effects during the study Severe renal failure (GFR < 30 ml/min) Uncontrolled diabetes or autonomic neuropathy History of neurological diseases or primary autonomic disorders (e.g., Parkinson’s disease) Use of antihypertensive medications that have a direct effect on orthostatic hypotension Inability or unwillingness of the patient to comply with follow-up

Design outcomes

Primary

MeasureTime frame
Improvement of systolic/diastolic blood pressure and symptom in standing position after 1 month of treatment with midodrine. Timepoint: Day 0: Measurement of blood pressure, assessment of orthostatic hypotension symptoms, and evaluation of patient quality of life.Day 7: Measurement of blood pressure, assessment of symptoms, and monitoring of adverse events.Day 14: Measurement of blood pressure, evaluation of treatment efficacy, and monitoring of adverse events.1 Month: Assessment of persistence of drug effects, monitoring of potential adverse events, and decision regarding continuation of therapy. Method of measurement: Supine Position: The patient remains in a supine position for at least 5 minutes, after which blood pressure and heart rate are measured and recorded.Immediately after Standing: The patient changes from supine to standing, and blood pressure and heart rate are measured during the first minute of standing.3 Minutes after Standing: While remaining in the standing position, blood pressure is measured again at the third minute.5 Minutes after Standing (optional): In some studies, blood pressure is also recorded at the fifth minute of standing.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHamed Bazrafshan Drissi

Shiraz University of Medical Sciences

hamedbazrafshan@sums.ac.ir+98 71 3627 6710

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026