Esophageal Achalasia Clinical Trial
Official title:
Different Surgical Procedures of Peroral Endoscopic Myotomy(POEM) for Esophageal Achalasia: a Multicenter Prospective Randomized Controlled Trial
This study compares the clinical efficacy of safety of circular myotomy and full-thickness myotomy guided by peroral endoscopic in treatment of incision length of ≤7cm and of ≥7cm in achalasia patients.
Status | Recruiting |
Enrollment | 400 |
Est. completion date | December 2021 |
Est. primary completion date | December 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility |
Inclusion Criteria: 1. Between 18 and 75 years of age; 2. Patient with esophageal achalasia; 3. Eckardt score > 3; 4. Signed informed consent. Exclusion Criteria: 1. Severe cardio-pulmonary disease or other serious disease leading to unacceptable surgical risk; 2. Pseudo-achalasia, Mega-oesophagus (greater than 7 cm), or Oesophageal diverticula in the distal oesophagus; 3. Previous endoscopic Botox injection; 4. Previous oesophageal or gastric surgery; 5. Pregnancy or lactation women, or ready to pregnant women; 6. Not capable of filling out questionnaires. |
Country | Name | City | State |
---|---|---|---|
China | Nanfang Hospital of Southern Medical University | Guanzhou | Guangdong |
Lead Sponsor | Collaborator |
---|---|
Nanfang Hospital of Southern Medical University |
China,
Boeckxstaens GE, Annese V, des Varannes SB, Chaussade S, Costantini M, Cuttitta A, Elizalde JI, Fumagalli U, Gaudric M, Rohof WO, Smout AJ, Tack J, Zwinderman AH, Zaninotto G, Busch OR; European Achalasia Trial Investigators.. Pneumatic dilation versus laparoscopic Heller's myotomy for idiopathic achalasia. N Engl J Med. 2011 May 12;364(19):1807-16. doi: 10.1056/NEJMoa1010502. — View Citation
Inoue H, Minami H, Kobayashi Y, Sato Y, Kaga M, Suzuki M, Satodate H, Odaka N, Itoh H, Kudo S. Peroral endoscopic myotomy (POEM) for esophageal achalasia. Endoscopy. 2010 Apr;42(4):265-71. doi: 10.1055/s-0029-1244080. Epub 2010 Mar 30. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Therapeutic success | Therapeutic success is defined as a symptom control to an Eckardt score of 3 or less. The Eckardt score is the sum of the symptom scores for dysphagia, regurgitation, and chest pain (with a score of 0 indicating the absence of symptoms, 1 indicating occasional symptoms, 2 indicating daily symptoms, and 3 indicating symptoms at each meal) and weight loss (with 0 indicating no weight loss, 1 indicating a loss of <5 kg, 2 indicating a loss of 5 to 10 kg, and 3 indicating a loss of >10 kg) (Eckardt, V. Gastroenterology, 1992. 103(6): p. 1732-8.) | From date of randomization until the follow-up ended, assessed up to 5 years | |
Secondary | Procedure related complication | Perforation, Delayed bleeding, Pneumothorax, Subcutaneous emphysema, Anastomotic leak etc. | From date of randomization until the follow-up ended, assessed up to 5 years | |
Secondary | Time of treatment failure | Time of treatment failure is defined as when the Eckardt score of patients are more than 3. | From date of randomization until the follow-up ended, assessed up to 5 years | |
Secondary | Pressure at the lower esophageal sphincter | From date of randomization until the follow-up ended, assessed up to 5 years | From date of randomization until the follow-up ended, assessed up to 5 years | |
Secondary | Quality of life | Patients will complete the quality-of-life questionnaires (the Medical Outcomes Study 36-Item Short-Form Health Survey, SF-36) for assessing quality of life. | From date of randomization until the follow-up ended, assessed up to 5 years |
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