A Randomized Comparison of Laparoscopic Myotomy and Pneumatic Dilatation for Achalasia
Esophageal Achalasia
About this trial
This is an interventional treatment trial for Esophageal Achalasia focused on measuring laparoscopic myotomy, pneumatic dilatation, motility disorder, dysphasia, health-related quality of life
Eligibility Criteria
Inclusion Criteria: Clinical diagnosis of achalasia by a physician manometric diagnosis of achalasia including both: Incomplete relaxation of the lower esophageal sphincter during swallowing (<80% of elevation over intragastric pressure and absence of esophageal peristalsis (peristalsis in <20% of initiated contractions) Facility with English, ability to complete English language questionnaires Exclusion Criteria: Pseudoachalasia: esophageal carcinoma; esophageal stricture; previous esophageal or gastric surgery; previous instrumentation of the lower esophageal sphincter i.e. suture, polymer injection, silicone band Previous gastric or esophageal surgery: fundoplication; Heller myotomy; gastric resection; vagotomy with or without gastric drainage Age 17 year or less Pregnancy Presence of severe comorbid illness: unstable angina; recent myocardial infarction (<6 months), cancer (except integumentary), unless free of disease for more than 5 years; end stage renal disease; previous stroke with cognitive, motor speech, or swallowing deficit persisting longer than one month; severe respiratory disease; cognitive impairment
Sites / Locations
- St. Michael's Hospital, 30 Bond Street, Suite 16 048 Cardinal Carter Wing
- University Health Network
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
1
2
pneumatic dilatation
Laparoscopic myotomy