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Endoscopic Versus Laparoscopic Myotomy for Treatment of Idiopathic Achalasia

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01601678
Acronym
POEMrct
Enrollment
240
Registered
2012-05-18
Start date
2012-12-31
Completion date
2023-05-30
Last updated
2023-06-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Achalasia

Keywords

Achalasia, Heller Myotomy, Dysphagia, Peroral Endoscopic Myotomy, LHM, POEM

Brief summary

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.

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.

Interventions

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.

PROCEDURELaparoscopic Heller Myotomy (LHM)

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.

Sponsors

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
CollaboratorOTHER
Karolinska University Hospital
CollaboratorOTHER
University Hospital Prague (IKEM), Prague, Czech Republic
CollaboratorUNKNOWN
Universitaire Ziekenhuizen KU Leuven
CollaboratorOTHER
Istituto Clinico Humanitas
CollaboratorOTHER
Wuerzburg University Hospital
CollaboratorOTHER
University Hospital Augsburg
CollaboratorOTHER
Universitätsklinikum Hamburg-Eppendorf
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Eckhard symptom scores2 years after treatmentAchalasia 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

Secondary

MeasureTime frameDescription
Treatment success rates3 and 6 months, and 1, 3, and 5 years post proceduresuccess rates result from Eckardt Scores
Manometry databefore, and 3 months, and 2 and 5 years post procedureAchalasia subtypes (before treatment) and assessment of lower esophagus sphincter function
Reflux score (clinical DeMeester score)before, and 3 and 6 months, and 1, 2, 3, and 5 years post procedureclinical DeMeester Reflux questionnaire to evaluate therapeutic side effects, range from 0 (no Reflux symptoms) to 6 (full symptom range).
Reflux symptomsbefore, and 3 and 6 months, and 1, 2, 3, and 5 years post procedureList of side effects due to reflux past POEM as short term and long term outcomes
pH metry3 months and 2 and 5 years after therapypH metry data after therapy
Adverse EventsBaseline to five years past procedurecomplication rate (Adverse Events (AE) and Serious Adverse Events (SAE))
Quality of Life indexbefore, and 3 months, and 2 and 5 years post procedureLife quality assessment (gastrointestinal LQ index by Eypasch, Wood-Dauphinee and Troidl) for individual success Evaluation (GIQLI), Best outcome score is 144.
EGD findings3 months and (optional) 2 and 5 years after therapyEGD findings to evaluate reflux effects after therapy
Eckhard symptom scoresbefore,and 3 and 6 months, 1,3 and 5 years past procedureAchalasia symptom questionnaire to evaluate individual therapy success, range from 0 (no Achalasia symptoms) to 12 (full symptom range)
Hb lab valuesday before procedure to day after procedureHemoglobin values measured in g/dl (grams per decilitre) pre and post procedure
Leucocyte lab valuesday before procedure to day after procedureLeucocyte values measured in billions per litre pre and post procedure, number of days of hospitalisation, myotomy length, duration of procedure
number of days of hospitalisationthrough inhouse stay after procedure, an average of 2-7 daysinhouse stay after procedure
myotomy lengthday of proceduremyotomy length in cm
duration of procedureday of procedureduration of procedure in minutes
Therapy failuresfrom procedure to 5 years after procedurenumber of therapy failures
Retreatmentsfrom procedure to 5 years after procedurenumber and kinds of retreatments
CRP lab valuesday before procedure to day after procedureCRP values measured in mg/l (milligrams per litre) pre and post procedure

Countries

Belgium, Czechia, Germany, Italy, Netherlands, Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026