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Clinical Trial Summary

This study aims to assess the efficacy and safety of linaclotide in patients with overlapping symptoms of both functional dyspepsia (FD) and constipation-predominant irritable bowel syndrome (IBS-C).


Clinical Trial Description

After being informed about the content and risks of the research, all eligible patients giving written informed consent will be randomly allocated in a 2:1 ratio to linaclotide (290μg, once daily) or lactulose (20mL, once daily). Treatment will last consecutively for 4 weeks, and patients' symptoms will be assessed before and after four-week treatment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05134584
Study type Interventional
Source RenJi Hospital
Contact Shengliang Chen
Phone 86-21-58752345
Email chenslmd@163.com
Status Recruiting
Phase Phase 4
Start date January 1, 2021
Completion date February 2022

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