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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03012854
Other study ID # NFEC-2016-186
Secondary ID
Status Recruiting
Phase N/A
First received January 5, 2017
Last updated May 11, 2017
Start date December 2016
Est. completion date December 2021

Study information

Verified date May 2017
Source Nanfang Hospital of Southern Medical University
Contact Wei Gong, Doctor
Phone 86-15820290385
Email drgwei@foxmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

Esophageal achalasia is an esophageal motor disorder, which is characterized by the absence of esophageal peristalsis combined with a defective relaxation of the lower esophageal sphincter (LES). The major symptoms of esophageal achalasia are dysphagia, chest pain, and regurgitation of undigested food.

Currently, treatment options mainly focus on relief of the symptoms by reducing the LES pressure. Pneumatic dilation is the main endoscopic therapies for esophageal achalasia. However, the patients need repeat treatment to maintain therapeutic success and there is a risk of perforation (1%-3%). For surgery approaches, the laparoscopic Heller's myotomy (LHM) combined with Dor's antireflux procedure has gained considerable interest. The LHM can sustain therapeutic effects for long-term in approximately 80% of patients.

Recently, Inoue et al. succeeded in treating achalasia endoscopically with a method called peroral endoscopic myotomy (POEM) and achieved promising results in short-term. Technically, POEM derived from natural orifice transluminal endoscopic surgery (NOTES) and endoscopic submucosal dissection (ESD), in which a submucosal tunnel is created after submucosal injection, and then an endoscopic myotomy was made at the gastroesophageal junction.

However, 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 were not determined, and there was no prospective study that compared different surgical procedures of POEM for esophageal achalasia. Therefore, we aim to compare 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.


Recruitment information / eligibility

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.

Study Design


Intervention

Procedure:
short-myotomy
Entry to submucosal space. After submucosal injection, a 2-cm longitudinal mucosal incision is made at approximately 8-10 cm proximal to the gastroesophageal junction (GEJ). Submucosal tunnelling. A long submucosal tunnel is created to 3 cm distal to the GEJ. Endoscopic myotomy is carried out in a proximal to distal direction to a total length less than 7 cm. The expected end point of myotomy is 2 cm distal to the GEJ. Myotomy of inner circular muscle bundles and outer longitudinal muscle layer is done. Closure of mucosal entry: the mucosal incision is closed using hemostatic clips.
long-myotomy
Entry to submucosal space. After submucosal injection, a 2-cm longitudinal mucosal incision is made at approximately 8-10 cm proximal to the gastroesophageal junction (GEJ). Submucosal tunnelling. A long submucosal tunnel is created to 3 cm distal to the GEJ. Endoscopic myotomy is carried out in a proximal to distal direction to a total length more than 7 cm. The expected end point of myotomy is 2 cm distal to the GEJ. Myotomy of inner circular muscle bundles and outer longitudinal muscle layer is done. Closure of mucosal entry: the mucosal incision is closed using hemostatic clips.
full-thickness myotomy
Entry to submucosal space. After submucosal injection, a 2-cm longitudinal mucosal incision is made at approximately 8-10 cm proximal to the gastroesophageal junction (GEJ). Submucosal tunnelling. A long submucosal tunnel is created to 3 cm distal to the GEJ. Endoscopic myotomy is carried out in a proximal to distal direction to a total length more than 7 cm. The expected end point of myotomy is 2 cm distal to the GEJ. Myotomy of inner circular muscle bundles and outer longitudinal muscle layer is done. Closure of mucosal entry: the mucosal incision is closed using hemostatic clips.
circular myotomy
Entry to submucosal space. After submucosal injection, a 2-cm longitudinal mucosal incision is made at approximately 8-10 cm proximal to the gastroesophageal junction (GEJ). Submucosal tunnelling. A long submucosal tunnel is created to 3 cm distal to the GEJ. Endoscopic myotomy is carried out in a proximal to distal direction to a total length more than 7 cm. The expected end point of myotomy is 2 cm distal to the GEJ. Myotomy of inner circular muscle bundles is done, leaving the outer longitudinal muscle layer intact. Closure of mucosal entry: the mucosal incision is closed using hemostatic clips.

Locations

Country Name City State
China Nanfang Hospital of Southern Medical University Guanzhou Guangdong

Sponsors (1)

Lead Sponsor Collaborator
Nanfang Hospital of Southern Medical University

Country where clinical trial is conducted

China, 

References & Publications (2)

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

Outcome

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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