Endoscopic Versus Laparoscopic Myotomy for Treatment of Idiopathic Achalasia (POEMrct)

June 27, 2023 updated by: Prof. Dr. Thomas Rösch, Universitätsklinikum Hamburg-Eppendorf

Endoscopic Versus Laparoscopic Myotomy for Treatment of Idiopathic Achalasia: A Randomized, Controlled Trial

Achalasia is a rare neurodegenerative esophageal motility disorder characterized by incomplete lower esophageal sphincter (LES) relaxation, increased LES tone, and aperistalsis of the esophagus leading to dysphagia, regurgitation, and chest pain. therapies for achalasia consist of endoscopic balloon dilatation (EBD) and botulinum toxin injection (EBTI), or surgical Treatment via i Heller Myotomy; surgery is nowadays mostly performed via the laparoscopic approach. Surgical therapy demonstrated superior treatment efficacy compared to EBD and EBTI. Recently, an endoscopic means to perform myotomy via a submucosal tunnel has been developed, namely PerOral Endoscopic Myotomy (POEM). Uncontrolled studies have indicated a symptomatic success rate of >90% for POEM in short term follow-ups.The aim of this study is to compare short and long-term feasibility, safety and efficacy of endoscopic (POEM) with laparoscopic myotomy (Heller myotomy) in the treatment of achalasia.

Study Overview

Detailed Description

Achalasia is considered a primary esophageal motility disorder which is defined as an insufficient relaxation of the lower esophageal sphincter. Incomplete lower esophageal sphincter (LES) relaxation, increased LES tone, and aperistalsis of the esophagus are characteristics of achalasia. Incidence peaks between ages 20 to 40. The most commonly reported symptoms are dysphagia (both for solids and liquids), regurgitation, and chest pain. The diagnosis is established with esophageal manometry and barium swallow radiographic studies and also with endoscopy being performed to exclude neoplastic or inflammatory diseases. Endoscopic therapies consist of either balloon dilatation (EBD) or Botulinum toxin injection (EBTI). The surgical treatment for achalasia is Heller Myotomy, nowadays almost exclusively performed laparoscopically.Superior to EBD and EBTI, surgical myotomy has shown sustained therapeutic efficacy in approximately 90% of patients which may be especially relevant for young patients with achalasia.

Recently an endoscopic technique to create myotomy via a submucosal tunnel has been developed, named PerOral Endoscopic Myotomy (POEM). The technique was first reported by Pasricha et al. in a porcine study, and Inoue et al. later reported the first clinical results in achalasia patients which showed significantly reduced dysphagia symptom scores and decreased resting lower esophageal sphincter (LES) pressures in 17 patients with a mean follow-up of 5 months . No serious complications related to POEM were encountered in this initial single-center trial. Several smaller pilot studies from Asia, Europe and USA have replicated the promising results regarding feasibility, safety and short-term efficacy,leading us to hope for a similar success rate along with reduced patient discomfort At present, POEM has the potential to be the first scarless flexible endosurgical intervention to become an established clinical treatment.The technique uses a submucosal esophageal tunnel through which a distal esophageal myotomy down to the proximal stomach is performed. For POEM to be integrated into clinical routine, comparative data regarding safety and efficacy are necessary.Our study group intends to compare safety and long-term efficacy of POEM to laparoscopic Heller myotomy, the current gold-Standard, in a non-inferiority design.

Patients with symptomatic achalasia and medical indication for interventional therapy will be randomized to either POEM therapy or standard laparoscopic Heller myotomy (with anti-reflux procedure)(LHM). They will be followed up closely in a defined time pattern evolving individual life quality and achalasia scores as well as clinical scores and diagnostics over a period of 5 years.

Due to considerations concerning the comparability to other achalsia Trials (Boeckxstaens,NEJM 2011), in November 2012 primary outcome has been changed to Eckardt Score instead of lower sphicter pressure. Amendment was done before patient inclusion started. Sample size was not affected by amendment.

Study Type

Interventional

Enrollment (Actual)

240

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Leuven, Belgium, 3000
        • University Hospital Leuven
      • Prague, Czechia
        • University Hospital Prague (IKEM)
      • Augsburg, Germany, 86156
        • Klinikum Augsburg,Klinik für Innere Medizin III
      • Hamburg, Germany, 20246
        • Universitätsklinikum Eppendorf
      • Würzburg, Germany, 97080
        • University Hospital Wurzburg
      • Rozzano, Italy
        • Istituto Clinico Humanitas
      • Amsterdam, Netherlands
        • Academic Medical Center
      • Stockholm, Sweden, S141 86
        • Ersta Hospital and Karolinska University Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

14 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Patients with symptomatic achalasia with an Eckardt score of > 3 and pre-op barium swallow, manometry and esophagogastroduodenoscopy consistent with the diagnosis
  • Persons of age > 18 years with medical indication for surgical myotomy or EBD
  • Signed written Informed Consent

Exclusion Criteria:

  • Patients with previous surgery of the stomach or esophagus
  • Patients with known coagulopathy
  • Previous surgical achalasia treatment
  • Patients with liver cirrhosis and/or esophageal varices
  • Active esophagitis
  • Eosinophilic esophagitis
  • Barrett's esophagus
  • Pregnancy
  • Stricture of the esophagus
  • Malignant or premalignant esophageal lesion
  • Severe Candida esophagitis
  • Hiatal hernia > 1cm
  • Extensive tortuous dilatation (>7cm luminal diameter, S shape) of the esophagus
  • Advanced malignant tumor with prognosis < 2 years

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Peroral Endoscopic Myotomy POEM
Patients with Achalasia, designated to receive a myotomy of the lower esophageal sphincter, who have been randomised into the POEM therapy group
After lavage, measure gastro-esophageal junction (GEJ) in cm from mouth piece. Determine entry point 12-14cm above GEJ at the lesser curvature site, inject 10ml coloured saline, create entry point. Advance endoscope into the submucosa, dissect the submucosal tunnel up to 2-3cm into the cardia. Dissect the submucosa close to the muscularis and check endoluminally for the direction of the lesser curvature, sufficient extension onto the cardia and mucosal integrity. After tunnel completion flush with gentamycin and saline. Start myotomy from proximally to distally starting 4-5cm below the mucosal entry site; the inner circular muscle layer should be fully dissected especially at the cardia for good symptomatic results. It is vital that the mucosa of the tubular esophagus remains intact. Extend myotomy at least 2cm onto the cardia. After completion check for mucosal integrity and opening of the distal esophageal sphincter. Close the entry point with clips from distal to proximal.
Active Comparator: Laparoscopic Heller Myotomy LHM
Patients with Achalasia, designated to receive a myotomy of the lower esophageal sphincter, who have been randomised into the LHM therapy group.
Use five trocar technique with patient in the French position as for laparoscopic anti-reflux procedures. Establish 12-15 mm Hg pneumoperitoneum. Use left paramedian trocar for camera, two lateral trocars for elevating liver and retraction of stomach and two trocars for dissection and suturing. Use of robotic surgery devices is allowed. Divide phrenoesophageal ligament starting on the right and mobilize distal esophagus on the lateral and anterior side. Identify and spare anterior vagal nerve. Perform myotomy by dividing both muscle-layers extending at least 6 cm above gastroesophageal junction and at least 2-3 cm inferiorly over stomach. Perform extent downwards after dividing epiphrenic fat pad overlying cardia. Measure myotomy length. Peroperative endoscopy check is advisable. Perform anterior fundoplication according to Dor. Only if necessary mobilize fundus of the stomach by dividing short gastric vessels. Suture fundus to both cut edges of myotomy, using non-resorbable material.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Eckhard symptom scores
Time Frame: 2 years after treatment
Achalasia symptom questionnaire to evaluate individual therapy success, range from 0 (no Achalasia symptoms) to 12 (full symptom range), treatment success is defined as an Eckardt Score ≤ 3
2 years after treatment

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Eckhard symptom scores
Time Frame: before,and 3 and 6 months, 1,3 and 5 years past procedure
Achalasia symptom questionnaire to evaluate individual therapy success, range from 0 (no Achalasia symptoms) to 12 (full symptom range)
before,and 3 and 6 months, 1,3 and 5 years past procedure
Treatment success rates
Time Frame: 3 and 6 months, and 1, 3, and 5 years post procedure
success rates result from Eckardt Scores
3 and 6 months, and 1, 3, and 5 years post procedure
Manometry data
Time Frame: before, and 3 months, and 2 and 5 years post procedure
Achalasia subtypes (before treatment) and assessment of lower esophagus sphincter function
before, and 3 months, and 2 and 5 years post procedure
Reflux score (clinical DeMeester score)
Time Frame: before, and 3 and 6 months, and 1, 2, 3, and 5 years post procedure
clinical DeMeester Reflux questionnaire to evaluate therapeutic side effects, range from 0 (no Reflux symptoms) to 6 (full symptom range).
before, and 3 and 6 months, and 1, 2, 3, and 5 years post procedure
Reflux symptoms
Time Frame: before, and 3 and 6 months, and 1, 2, 3, and 5 years post procedure
List of side effects due to reflux past POEM as short term and long term outcomes
before, and 3 and 6 months, and 1, 2, 3, and 5 years post procedure
pH metry
Time Frame: 3 months and 2 and 5 years after therapy
pH metry data after therapy
3 months and 2 and 5 years after therapy
Adverse Events
Time Frame: Baseline to five years past procedure
complication rate (Adverse Events (AE) and Serious Adverse Events (SAE))
Baseline to five years past procedure
Quality of Life index
Time Frame: before, and 3 months, and 2 and 5 years post procedure
Life quality assessment (gastrointestinal LQ index by Eypasch, Wood-Dauphinee and Troidl) for individual success Evaluation (GIQLI), Best outcome score is 144.
before, and 3 months, and 2 and 5 years post procedure
EGD findings
Time Frame: 3 months and (optional) 2 and 5 years after therapy
EGD findings to evaluate reflux effects after therapy
3 months and (optional) 2 and 5 years after therapy
CRP lab values
Time Frame: day before procedure to day after procedure
CRP values measured in mg/l (milligrams per litre) pre and post procedure
day before procedure to day after procedure
Hb lab values
Time Frame: day before procedure to day after procedure
Hemoglobin values measured in g/dl (grams per decilitre) pre and post procedure
day before procedure to day after procedure
Leucocyte lab values
Time Frame: day before procedure to day after procedure
Leucocyte values measured in billions per litre pre and post procedure, number of days of hospitalisation, myotomy length, duration of procedure
day before procedure to day after procedure
number of days of hospitalisation
Time Frame: through inhouse stay after procedure, an average of 2-7 days
inhouse stay after procedure
through inhouse stay after procedure, an average of 2-7 days
myotomy length
Time Frame: day of procedure
myotomy length in cm
day of procedure
duration of procedure
Time Frame: day of procedure
duration of procedure in minutes
day of procedure
Therapy failures
Time Frame: from procedure to 5 years after procedure
number of therapy failures
from procedure to 5 years after procedure
Retreatments
Time Frame: from procedure to 5 years after procedure
number and kinds of retreatments
from procedure to 5 years after procedure

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Thomas Roesch, Prof., Interdisciplinary Endoscopy Department and Clinic, University Hospital Hamburg-Eppendorf, Germany
  • Principal Investigator: Paul Fockens, Prof., Department of Gastroenterology and Hepatology, Academic Medical Center, Amsterdam; Netherlands
  • Principal Investigator: Bengt Håkanson, Prof., Department of Surgery, Karolinska University Hospital, Stockholm, Sweden
  • Principal Investigator: Guy Boeckxstaens, Prof., Universitaire Ziekenhuizen KU Leuven
  • Principal Investigator: C.T. Germer, Prof., Wuerzburg University Hospital
  • Principal Investigator: Riccardo Repici, Prof., Istituto Clinico Humanitas, Rozzano, Italy
  • Principal Investigator: Uberto Fumagalli, Prof., Istituto Clinico Humanitas, Rozzano, Italy
  • Principal Investigator: Julius Spicak, Prof., University Hospital Prague, Prague, Czech Republic
  • Principal Investigator: Helmut Messmann, Prof., Department for Internal Medicine III, Klinikum Augsburg, Germany

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 1, 2012

Primary Completion (Actual)

May 30, 2022

Study Completion (Actual)

May 30, 2023

Study Registration Dates

First Submitted

May 15, 2012

First Submitted That Met QC Criteria

May 16, 2012

First Posted (Estimated)

May 18, 2012

Study Record Updates

Last Update Posted (Actual)

June 28, 2023

Last Update Submitted That Met QC Criteria

June 27, 2023

Last Verified

June 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • POEM vs. LHM
  • PV 4133 (Registry Identifier: Hamburg Chamber of Physicians)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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