Baclofen for Rumination

Status Completed

Clinical Trial Summary

Patients with a clinical suspicion of rumination syndrome and/or supra-gastric belching are randomized into baclofen or placebo for 2 weeks (10mg, tid). thereafter, they undergo a high resolution impedance manometry measurement, were they receive a solid meal, and recordings continue for another hour. Thereafter, they will receive the alternative treatment, after which they will undergo a second high resolution impedance manometry measurement. Patients are asked to fill out questionnaires during the entire study period.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Feeding and Eating Disorders of Childhood
Rumination
Supra-gastric Belching

Clinical Trial Details

NCT number	NCT03113396
Study type	Interventional
Source	Universitaire Ziekenhuizen Leuven
Contact
Status	Completed
Phase	Phase 4
Start date	February 1, 2012
Completion date	December 31, 2016

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