Trial Details

COMPLETED
Basic Information
Clinical ID c4396
Identifier NCT00584571
Trial Title SAT vs Escitalopram for Rectal Hypersensitivity
Trial URL Visit Original Page
Study Information
Study Results

NO

Conditions Rectal Hypersensitivity|Irritable Bowel Syndrome-Constipation
Interventions PROCEDURE: Sensory Adaptation Training|DRUG: Escitalopram Therapy
Participant Information
Sponsor Augusta University
City Augusta
Country/Region United States
Enrollment Criteria
Sex Requirement ALL
Age Requirement ADULT, OLDER_ADULT
Study Design
Study Type INTERVENTIONAL
Phase PHASE2
Time Information
Start Date 2007-12
Primary Completion Date 2015-12-31
Completion Date 2019-12-31