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RECRUITING
NCT06761443
NA

To Evaluate the Safety and Efficacy of Pediococcus Acidilactici PA53 in Relieving Constipation in Adults

Sponsor: Wecare Probiotics Co., Ltd.

View on ClinicalTrials.gov

Summary

To study the improvement of constipation symptoms, quality of life and mental state, intestinal function, intestinal hormones, inflammation and immunity, and intestinal flora of constipation subjects after 8-week intervention with Pediococcus acidilactici PA53.

Official title: Based on a Randomized, Double-blind, Placebo-controlled Trial, we Evaluated the Safety and Efficacy of Pediococcus Acidilactici PA53 in Relieving Constipation in Adults

Key Details

Gender

All

Age Range

18 Years - 70 Years

Study Type

INTERVENTIONAL

Enrollment

10

Start Date

2025-02-25

Completion Date

2025-05-25

Last Updated

2025-01-07

Healthy Volunteers

Yes

Conditions

Interventions

DIETARY_SUPPLEMENT

Probiotic

The experimental phase of this study had last 8 weeks and each patient will make 3 visits (week 0, week 4, week 8).

DIETARY_SUPPLEMENT

Maltodextrin

The experimental phase of this study had last 8 weeks and each patient will make 3 visits (week 0, week 4, week 8).

Locations (1)

Department of Nutrition, General Hospital of Ningxia Medical University

Yinchuan, Ningxia, China