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Midodrine Versus Placebo in VasoVagal Syncope

Prospective Evaluation of the Midodrine Efficacy in the Treatment of Vasovagal Syncope: A Randomized Placebo-Controlled Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT138803061965N1
Enrollment
100
Registered
2009-09-15
Start date
2006-07-14
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Vasovagal syncope. Syncope and collapse

Interventions

Intervention 1: Midodrine 5 mg tid if neccessary 10 mg tid for one year. Intervention 2: Placebo 5 mg tid if neccessary 10 mg tid for one year.
Treatment - Drugs
Midodrine 5 mg tid if neccessary 10 mg tid for one year
Placebo 5 mg tid if neccessary 10 mg tid for one year

Sponsors

Research department of Rajaie Cardiovascular Medical and Research Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: (1) a frequency of at least one episode of syncope during previous 6-month and (2) a positive head-up tilt test. Exclusion criteria: (1) other causes of syncope; (2) cardiovascular and /or systemic disease; or (3) systolic blood pressure >150 mmHg or diastolic blood pressure >95 mmHg; or (4) thyrotoxicosis; or (5) renal failure; or (6) pheochromocytoma.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Syncope recurrence. Timepoint: 6-monthe and one year after treatment. Method of measurement: History.

Secondary

MeasureTime frame
Satisfaction score. Timepoint: 6-month and one year after treatment. Method of measurement: History (score 0=no response, score 6=excellent response).;Quality of life. Timepoint: 6-month and one year after treatment. Method of measurement: Endicott quality of life questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Human Bakhshandeh

Rajaie Cardiovascular Medical and Research Center

bakhshandeh@rhc.ac.ir+98 21 2392 2163

Outcome results

None listed

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