Trial Details

TERMINATED
Basic Information
Clinical ID c2533
Identifier NCT03336034
Trial Title Assessment of Responsiveness to Treatment by Experience Sampling Method
Trial URL Visit Original Page
Study Information
Study Results

NO

Conditions Constipation-predominant Irritable Bowel Syndrome
Interventions -
Participant Information
Sponsor Maastricht University Medical Center
City Maastricht
Country/Region Netherlands
Enrollment Criteria
Sex Requirement ALL
Age Requirement ADULT, OLDER_ADULT
Study Design
Study Type OBSERVATIONAL
Phase NULL
Time Information
Start Date 2018-01-01
Primary Completion Date 2022-05-01
Completion Date 2022-05-01