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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02073578
Other study ID # 2011H0240
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 2012
Est. completion date December 2014

Study information

Verified date September 2021
Source Ohio State University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a pilot study for a new endoscopic treatment of achalasia. Up to 25 patients will be recruited for this trial, with the intent to treat 20 patients.


Description:

This is a pilot study for a new endoscopic treatment of achalasia. Up to 25 patients will be recruited for this trial, with the intent to treat or attempt to treat 20 patients. Patients for whom a POEM has been attempted but not completed (conversion to open or laparoscopic surgery, POEM surgery aborted and not re-attempted). Patients who proceed to study treatment will undergo ten years of follow-up as part of this study.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date December 2014
Est. primary completion date September 2014
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Diagnosis of Achalasia - Age 16-80 - ASA Class 1-3 Exclusion Criteria: - Pregnancy - Any prior surgical or endoscopic treatment for achalasia -- first eight subjects. After eight subjects have been treated as part of this study, this exclusion criteria no longer applies - Patients who are taking immunosuppressive medications or are immunocompromised - Patients on anticoagulant medications or abnormal coagulation tests - Patients with severe medical comorbidities, in the judgment of the treating surgeon

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Peroral Endoscopic Myotomy (POEM)
Endoscopy myotomy for treatment of achalasia

Locations

Country Name City State
United States The Ohio State University Wexner Medical Center Columbus Ohio

Sponsors (1)

Lead Sponsor Collaborator
Ohio State University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Safety and Efficacy of POEM Procedure To assess adverse events related to POEM Intraoperative to one year follow-up
Primary Long-term patient-reported quality of life To assess change in quality of life from baseline, based on validated quality of life measures, at baseline through 1 year follow-up. Baseline to one year follow-up
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