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RECRUITING
NCT07462481
NA

Probiotic Improve Constipation

Sponsor: Wecare Probiotics Co., Ltd.

View on ClinicalTrials.gov

Summary

To evaluate the efficacy and safety of probiotic as a food supplement in regulating bowel habits in patients with chronic constipation, and to compare it with placebo.

Official title: A Randomized, Double-Blind, Placebo-Controlled Trial to Evaluate the Efficacy and Safety of Probiotics in Relieving Constipation in Adults

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

105

Start Date

2026-06-10

Completion Date

2027-08-01

Last Updated

2026-06-09

Healthy Volunteers

Yes

Conditions

Interventions

DIETARY_SUPPLEMENT

Probiotic

The intervention period of this study will last for 8 weeks (56 days), during which each participant will attend three study visits scheduled at baseline (Week 0), Week 4, and Week 8.

DIETARY_SUPPLEMENT

Placebo

The intervention period of this study will last for 8 weeks (56 days), during which each participant will attend three study visits scheduled at baseline (Week 0), Week 4, and Week 8.

DIETARY_SUPPLEMENT

High-activity probiotic probiotic

The intervention period of this study will last for 8 weeks (56 days), during which each participant will attend three study visits scheduled at baseline (Week 0), Week 4, and Week 8.

Locations (1)

Suzhou Ninth People's Hospital

Suzhou, Jiangsu, China