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Ivabradine effect on ventricular rate in non-paroxysmal atrial fibrillation patients

Comparison of Ivabradine effect versus placebo on ventricular rate in patients with non-paroxysmal atrial fibrillation under standard medical treatment

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20191230045950N2
Enrollment
100
Registered
2022-04-10
Start date
2022-02-20
Completion date
Unknown
Last updated
2022-05-02

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

Conditions

Atrial fibrilation. Persistent atrial fibrillation

Interventions

Intervention 1: Intervention group: Patients in this group are prescribed Ivabradine at a dose of 5 mg twice a day (manufactured by Kobel Daroo Company) for one month.24 hours ambulatory heart rhythm

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Non-paroxysmal atrial fibrillation at randomization, with no prospect of cardioversion, anti arrhythmic treatment with group I or III drugs, or pulmonary vein ablation Beta-blocker or nondihydropyridine calcium channel blocker or digoxin therapy at the maximum dose recommended for or tolerated by the patient Ventricular rate of more than 70 Be able to voluntarily give informed consent

Exclusion criteria

Exclusion criteria: Medical causes that explain poor heart rate control: fever, anemia, hyperthyroidism ,etc Patients with a known contraindication to Ivabradine Valve disease requiring surgical or percutaneous repair Impossibility to attend the visits scheduled in the protocol

Design outcomes

Primary

MeasureTime frame
Ventrical rate in non-paroxysmal atrial fibrillation patients. Timepoint: Before and one month after intervention. Method of measurement: 24 hours ambulatory heart rhythm monitoring.

Secondary

MeasureTime frame
Mean daytime ventricular rate. Timepoint: Before and one month after intervention. Method of measurement: 24 hours ambulatory heart rhythm monitoring.;Mean night time ventricular rate. Timepoint: Before and one month after intervention. Method of measurement: 24 hours ambulatory heart rhythm monitoring.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyede Houra Yeganegi

Shahid Beheshti University of Medical Sciences

Sarvenaz_yeganegi@yahoo.com+98 21 5541 9008

Outcome results

None listed

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