Chronic Idiopathic Constipation (CIC) Clinical Trials

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Assessing the Safety and Effectiveness of Weizmania Coagulant BC99 in Relieving Functional Constipation in Adults Based on Randomized, Double-Blind, Placebo-Controlled Trials

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Dietary supplement
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

To investigate the clinical effects of probiotics in relieving chronic constipation in adults, and evaluate the improvement of symptoms in patients with constipation as well as their impacts on gastrointestinal function, immunity, and gut microbiota.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 70
Healthy Volunteers: t
View:

• Chinese adults who meet the diagnostic criteria of Rome III, aged between 18 and 70;

• Patients with chronic constipation (disease duration exceeding 6 months, with fewer than 3 bowel movements per week and/or Bristol stool form scale types 1 and 2);

• Able to complete the study according to the requirements of the experimental protocol;

• Patients who have signed the informed consent form;

• Research participants (including male participants) who do not have fertility plans from 14 days before screening to 6 months after the end of the trial and are willing to take effective contraceptive measures voluntarily.

Locations
Other Locations
China
Henan University of Science and Technology
RECRUITING
Luoyang
The School of Food and Bioengineering, Henan University of Science and Technolog
RECRUITING
Luoyang
Contact Information
Primary
Ying Wu
wuying2000@126.com
18639283502
Time Frame
Start Date: 2024-05-30
Estimated Completion Date: 2024-11-15
Participants
Target number of participants: 100
Treatments
Experimental: Probiotic Group
Participants receive one sachet per day containing probiotic BC99 and maltodextrin (Week 0 to Week8).
Placebo_comparator: Placebo Group
Participants receive one sachet per day containing maltodextrin only, serving as the placebo(Week 0 to Week8).
Related Therapeutic Areas
Sponsors
Leads: Wecare Probiotics Co., Ltd.

This content was sourced from clinicaltrials.gov