Trials / Completed
CompletedNCT05803161
Congrong Runtong Oral Liquid in the Treatment of Functional Constipation (Yang-deficiency Type)
A Randomized, Double-blind, Dose-exploration, Parallel-controlled, Multicenter Phase II Clinical Study of Congrong Runtong Oral Liquid in the Treatment of Functional Constipation (Yang-deficiency Type)
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 180 (actual)
- Sponsor
- Beijing Hospital of Traditional Chinese Medicine · Academic / Other
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
Using a placebo as a control, this study aims to preliminarily evaluate the clinical efficacy of Congrong Runtong oral liquid for the treatment of functional constipation (Yang-deficiency type), explore the optimal dosage of Congrong Runtong oral liquid for functional constipation (Yang-deficiency type) to provide a basis for dosage selection in Phase III clinical trials, and observe the safety of clinical use of Congrong Runtong oral liquid.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Congrong Runtong oral liquid | Congrong Runtong oral liquid:component "total glycosides of Cistanche" extracted and refined from the traditional Chinese medicine Cistanche deserticola |
| DRUG | Placental Congrong Runtong oral liquid | Placental Congrong Runtong oral liquid |
Timeline
- Start date
- 2023-03-29
- Primary completion
- 2024-04-01
- Completion
- 2024-04-01
- First posted
- 2023-04-07
- Last updated
- 2024-10-28
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT05803161. Inclusion in this directory is not an endorsement.