Skip to content

A clinical trial to study the effects of two drugs Ivabradine and metoprolol in patients of Mitral Stenosis with Sinus Rhythm

Ivabradine vs beta blockers in Mitral Stenosis in Sinus Rhythm - METIVA trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/07/026401
Enrollment
60
Registered
2020-07-06
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: I050- Rheumatic mitral stenosis

Interventions

Intervention1: Ivabradine: 5 mg twice daily for 6 months Control Intervention1: Metoprolol: Metoprolol 50 mg once daily 6 month

Sponsors

VIMSAR
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age >=18 yrs. Documented/newly diagnosed mitral stenosis Normal sinus rhythm (heart rate not less than 70 bpm)

Exclusion criteria

Exclusion criteria: Unable to perform treadmill test (TMT)/contraindication for TMT/ Very severe MS in urgent need for surgical treatment Other significant valvular lesions (more than mild aortic stenosis/aortic regurgitation/ mitral regurgitation/Tricuspid regurgitation/Tricuspid stenosis) o Presence of significant noncardiac comorbidities, e.g., chronic obstructive pulmonary disease, renal failure, malignancy, etc. RHD with Pregnancy Known allergy/intolerance to study drugs known coronary artery disease, cardiomyopathies, congenital heart diseases, HTN etc. LVEF less than 40% Marked anaemia (Hb

Design outcomes

Primary

MeasureTime frame
To compare the efficacy of Ivabradine to Beta-blockers in terms of subjective and objective (clinical and hemodynamic and exercise) parameters between two groups.Timepoint: 6 months from reruitment

Secondary

MeasureTime frame
safety data-to document any adverse drug reactions related to drug ivabradine.Timepoint: 6months

Countries

India

Contacts

Public ContactDr Ayan Roy

Associate professor

drsasi12@gmail.com9337640488

Outcome results

None listed

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