NCT04640753
Peroral Endoscopic Myotomy for the Treatment of Achalasia
Recruiting
Not specifiedAges 18+ObservationalMethodist Health SystemInvestigator-initiated
~200 participants
Updated 2026-06-10 on ClinicalTrials.gov
What's tested:Endoscopic procedure for achalasia
At a glance
Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Decrease or no symptoms of chest pain
Measured over upto 180 days
Conditions
Where it's being run
1 sites across 1 statesTexas1
Study leadership
- Prashant Kedia, M.D. · PRINCIPAL_INVESTIGATOR · The Methodist Hospital Research Institute
Who to contact
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Do you actually qualify for this trial?
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Eligibility criteria
Inclusion
Any discharged patient who has undergone clinically indicated and/or standard of care POEM for the treatment of Achalasia from 6/2016 to 6/2021.
Above or equal to 18 years of age
Exclusion
Any patient who has not undergone POEM for the treatment of Achalasia.
Below 18 years of age
What this trial measures
- Decrease or no symptoms of chest painupto 180 days
To continue and review our treatment outcomes, patient safety in cases with achalasia, we follow up after the procedure up to 180 days. Follow-up period varies from patient to patient.