At a glance
ClinicalIndex Comparison RecordN/ACompleted· 60 enrolled
Drug / intervention
Short Myotomy +1 moreprocedure
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Outcomes of Short-length vs Standard-length Myotomy Using Per-Oral Endoscopic Myotomy (POEM) for Achalasia: A Randomized Controlled Pilot Study
In Brief
A clinical study evaluating Short Myotomy and Standard Length Myotomy for Achalasia. Completed, enrolled 60 participants across 1 site.
Detailed Summary
The objective of this randomized controlled trial (non-inferiority study) is to evaluate the outcomes of 4 cm short myotomy compared to the 8 cm standard length myotomy in Per-Oral Endoscopic Myotomy (POEM) for patients with achalasia. We hypothesize that a shorter myotomy with POEM will have the same clinical efficacy as standard length myotomy based on patient-reported Eckardt score with shorter procedure times and reduced complications.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsAchalasia
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
202120222023202420252026
Enrollment StartJun 2020
First PostedMar 2021
Primary CompletionFeb 2024
TodayJul 2026
First PostedMar 15, 2021
Enrollment StartJun 1, 2020
Primary CompletionFeb 29, 2024
TodayJul 2, 2026
Enrollment to primary: 3.7 yearsPosted 5.3 years ago
Interventions
Short Myotomyprocedure
Evaluation of short length myotomy
Standard Length Myotomyprocedure
Standard Length Myotomy