Clinical Trials Directory

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

TypeNameDescription
DRUGCongrong Runtong oral liquidCongrong Runtong oral liquid:component "total glycosides of Cistanche" extracted and refined from the traditional Chinese medicine Cistanche deserticola
DRUGPlacental Congrong Runtong oral liquidPlacental 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.