Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-24 @ 10:13 PM
Ignite Modification Date: 2025-12-24 @ 10:13 PM
NCT ID: NCT00802035
Eligibility Criteria: Inclusion Criteria: * Between the ages of 18 and 65 years * Body mass index of 19 to 30 kg/m2 at screening * If subject is female and of childbearing potential, she must agree to use an acceptable method of contraception for the duration of the study Exclusion Criteria: * Pregnancy and/or currently breastfeeding * Clinical significant medical condition or observed abnormalities * Acute gastrointestinal disorder or history of chronic gastrointestinal disease or surgery * Participation in a clinical trial within 30 days before screening * Known intolerance and/or hypersensitivity to baclofen or its excipients * Use of alcohol-, caffeine-, or xanthine-containing products * Clinically significant illness within 30 days of first study drug administration * Dietary restrictions that conflict with required study meals
Healthy Volunteers: True
Sex: ALL
Minimum Age: 18 Years
Maximum Age: 65 Years
Study: NCT00802035
Study Brief:
Protocol Section: NCT00802035