drugset / Trial / NCT05803161
Congrong Runtong Oral Liquid in the Treatment of Functional Constipation (Yang-deficiency Type)
RandomizedParallel-groupQuadruple-blindTreatment
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.
Timeline
- Start
- 2023-03-29
- Primary completion
- 2024-04-01
- Completion
- 2024-04-01
Outcome
Met primary endpoint
paper p < 0.0001 for 6g/d vs placebo PMID 41759423 ↗
paper p = 0.044 for 3g/d vs placebo PMID 41759423 ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Congrong Runtong oral liquid | Unknown | 1 g | Oral |
| Subject | Congrong Runtong oral liquid | Unknown | 2 g | Oral |