Clinical Trials Directory

Trials / Completed

CompletedNCT01525732

Per-Oral Endoscopic Myotomy (P.O.E.M.) for Treatment of Esophageal Motility Disorders

Prospective Study on the Feasibility and Effectiveness of Per-Oral Endoscopic Myotomy (P.O.E.M.) for Treatment of Primary Esophageal Motility Disorders

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
50 (actual)
Sponsor
Chinese University of Hong Kong · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Spastic esophageal motility disorders induced significant symptoms including dysphagia, retrosternal pain and regurgitation. Per oral endoscopic myotomy (P.O.E.M.) is a novel approach to perform myotomy through the esophagus with long submucosal tunnel. This study aimed to investigate the feasibility and safety of P.O.E.M. and translate the techniques from animal study to clinical practice in human.

Conditions

Interventions

TypeNameDescription
PROCEDUREPer Oral Endoscopic Myotomy

Timeline

Start date
2010-06-01
Primary completion
2017-04-25
Completion
2017-04-25
First posted
2012-02-03
Last updated
2017-05-01

Locations

1 site across 1 country: Hong Kong

Source: ClinicalTrials.gov record NCT01525732. Inclusion in this directory is not an endorsement.