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Study identifier: NCT05519683 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Home Transcutaneous Electrical Acustimulation (TEA)

Condition: Irritable Bowel Syndrome With Constipation  ·  Sponsor: University of Michigan

PhasePhase 2/Phase 3
Planned participants160
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This study will assess the efficacy of two active treatments with TEA and a chemical neuromodulator (escitalopram aka Lexapro) versus a sham comparator or control group on abdominal pain.

This description comes directly from the study's public registry record.

Talk to the study team

Colin Burnett  ·  734-647-2806  ·  bucolin@med.umich.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of MichiganAnn Arbor, Michigan, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05519683