Clinical Trial Details


Research Study Summary

Second Phase 3 Randomized, 12-Week, Double-Blind, Placebo-Controlled Study of the Safety and Efficacy of XXXXXX in Patients with Irritable Bowel Syndrome with Constipation (IBS-C)


A 12-week research study to test the safety and effectiveness of an investigational medication for the treatment of Irritable Bowel Syndrome with Constipation.

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CW ID: 213917
Date Last Changed: March 31, 2016

Clinical Trial Snapshot

Both Male and Female
18 to 85 Years
Overall Status
18 Weeks
Facility Type
Up to $450


Eligibility Criteria
  • Between 18 to 85 years old
  • Currently experiencing abdominal pain and constipation from IBS
  • Complete daily reports on your symptoms throughout the study
  • Be able to participate for approximately 18 weeks


Jennifer Wu, Clinical Research Coordinator
IMA Research
80-02 Kew Gardens Road, Suite 102
Kew Gardens, NY 11415
Phone: 866-879-2507 Ext. 711
Fax: 866-600-5303

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Research Center Information:

IMA Research

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