Trials / Unknown
UnknownNCT01750775
Shensongyangxin Capsule in the Treatment of Sinus Bradycardia With Premature Ventricular Contractions
Shensongyangxin Capsule in the Treatment of Sinus Bradycardia With Premature Ventricular Contractions Multi-center,Randomized, Double-blind, Placebo-controlled Clinical Study
- Status
- Unknown
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 330 (estimated)
- Sponsor
- kejiang Cao · Academic / Other
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to assess the effects of Chinese medicine Shansong Yangxin capsule for sinus bradycardia complicated with ventricular premature beats.
Detailed description
Premature ventricular contractions is one of the most common symptomatic arrhythmia. Antiarrhythmia drugs for premature ventricular contractions, such as beta-blockers and sodium channel blockers, can cause bradycardia. For sinus bradycardia patients complicated with premature ventricular contractions, it's hard for doctors to make decision. The purpose of the study is to assess the effects of Chinese medicine Shansong Yangxin capsule for sinus bradycardia complicated with ventricular premature beats, which based on the numbers of premature ventricular contractions and average hear rate in 24-hour ambulatory electrocardiogram (ECG) after 8 weeks treatment as the primary endpoint of the study. Secondary endpoints are evaluation of the Shensong Yangxin capsule on quality of life. This study is a randomized, double-blind, placebo controlled, multi-center trial. Sinus bradycardia patients(average heart rate 45-59 beat per minute) associated with premature ventricular contractions (PVC number \>10000 / 24h), are involved in the study. Patients are randomly assigned into Shensong Yangxin capsule group or placebo group, with the capsule administration of 4 granules t.i.d.for 8 weeks. 24-hour ambulatory ECG, are observed at baseline,4 weeks and 8 weeks after the intervention. The primary outcomes are the numbers of premature ventricular contractions and average heat rate in 24-hour ambulatory ECG, and the secondary outcomes is Minnesota living with heart failure questionnaire (MLHFQ).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Shensong Yangxin capsule | ShenSongYangXin Capsule 4 granules t.i.d. by mouth for 8 weeks |
| DRUG | placebo Capsule | placebo Capsule 4 granules t.i.d. by mouth for 8 weeks |
Timeline
- Start date
- 2012-08-01
- Primary completion
- 2013-09-01
- Completion
- 2013-12-01
- First posted
- 2012-12-17
- Last updated
- 2012-12-17
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT01750775. Inclusion in this directory is not an endorsement.