Trials / Not Yet Recruiting
Not Yet RecruitingNCT06669169
Efficacy and Safety of Jia Shen Tablets in Chronic Heart Failure
A Randomized, Placebo-Controlled, Double-Blind and Multi-Centre Phase II Clinical Trial:Efficacy and Safety of Jia Shen Tablets in the Treatment of Coronary Heart Disease Complicating Chronic Heart Failure (Syndrome of Yang Qi Deficiency With Blood Stasis)
- Status
- Not Yet Recruiting
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 288 (estimated)
- Sponsor
- Tasly Pharmaceutical Group Co., Ltd · Industry
- Sex
- All
- Age
- 40 Years – 79 Years
- Healthy volunteers
- Not accepted
Summary
Evaluate the efficacy and safety of Jia Shen Tablets in patients with Chronic Heart Failure.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Jia Shen Tablet Placebo | Jia Shen Tablet Placebo contains 4 placebo tablets (0.47 g per placebo tablet),take orally, 2 times a day for 12 weeks |
| DRUG | Low dose Jia Shen Tablet | Low dose Jia Shen Tablet contains 2 tablets (0.47 g per tablet) and 2 placebo tablets (0.47 g per placebo tablet),take orally, 2 times a day for 12 weeks |
| DRUG | High dose Jia Shen Tablet | High dose Jia Shen Tablet contains 4 tablets (0.47 g per tablet),take orally, 2 times a day for 12 weeks |
Timeline
- Start date
- 2025-01-31
- Primary completion
- 2026-12-31
- Completion
- 2026-12-31
- First posted
- 2024-11-01
- Last updated
- 2024-11-01
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT06669169. Inclusion in this directory is not an endorsement.