drugset / Trial / NCT05803161

Congrong Runtong Oral Liquid in the Treatment of Functional Constipation (Yang-deficiency Type)

NCT05803161 ↗

Phase 2 Completed 180 enrolled Beijing Hospital of Traditional Chinese Medicine
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

EvaluationDrugModalityDoseRoute
Subject Congrong Runtong oral liquid Unknown 1 g Oral
Subject Congrong Runtong oral liquid Unknown 2 g Oral

Indications