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Study identifier: NCT06835374 Synced from ClinicalTrials.gov · July 29, 2026
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Comparative Assessment of Esophagitis in Cases With and Without Esophageal Motility Disorders: A Prospective Study

Condition: Esophageal Diseases  ·  Sponsor: Asian Institute of Gastroenterology, India

PhaseNA
Planned participants200
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

Achalasia is a neuro-degenerative disorder marked by changes in the peristalsis of the esophagus and the lack of relaxation in the lower esophageal sphincter (LES), thought to be due to damage to the myenteric plexus with an unknown cause.1 Per-oral endoscopic myotomy (POEM) is an established endoscopic treatment modality for achalasia. Leading gastrointestinal (GI) societies endorse POEM as one of the primary treatment option for achalasia.This study aims to characterize and compare the morphological characteristics of reflux related erosions after the POEM procedures versus those in cases without esophageal motility disorders. Data collection 1. Demographic characteristics: Age, gender, type of achalasia 2. Manometry findings (pre and post POEM): integrated relaxation pressure, lower esophageal sphincter pressure 3. Comorbidities 4. Medications 5. Eckardt score: before procedure and 3-months after Procedure 6. POEM procedure details: length of esophageal and gastric myotomy, adverse events, length of hospital stay 7. Evaluation at 3-months Symptom: standardized questionnaire (GERDQ) Endoscopy: grade of esophagitis Erosions vs ulcers Dimension of erosions Anatomical location (according to clock)

This description comes directly from the study's public registry record.

Talk to the study team

Rajesh Goud Mr Maragoni, M.Pharm, MBA  ·  04023378888  ·  rajeshgoud761@gmail.com

Zaheer Nabi Dr Mohammed, MBBS MD  ·  04023378888  ·  zaheernabi1978@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Asian Institute of Gastroenterology HospitalHyderabad, Telangana, IndiaRecruiting

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Source record: clinicaltrials.gov/study/NCT06835374