Comparison of Long-term Success Rates of POEM With LHM Clinical Trial
— POEM3Official title:
Comparison of Peroral Endoscopic Myotomy (POEM) With Laparoscopic Heller Myotomy (LHM) for Treatment of Achalasia, a Retrospective Multicenter Study
Verified date | June 2019 |
Source | Universitätsklinikum Hamburg-Eppendorf |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
For the treatment of Achalasia, LHM has been the only surgical therapy. Recently, an endoscopic approach for this therapy has been developed (peroral endoscopic Myotomy POEM). Studies show promising short and mid term results for POEM. At present, POEM is considered a promising new technique with the potential to become a standard achalasia treatment. For this to happen, long-term comparative data with LHM is required. Therefore,the intention for this study is to investigate the short and long-term efficacy of POEM for the treatment of achalasia as it was performed in international centers and compare outcomes with database assessment of LHM.
Status | Terminated |
Enrollment | 47 |
Est. completion date | December 2014 |
Est. primary completion date | December 2014 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Patients with symptomatic achalasia and pre-op barium swallow, manometry and oesophago-gastro-duodenoscopy which have been consistent with the diagnosis - Age > 18 years with medical indication for interventional achalasia treatment - Availability of Eckardt score at baseline and 12 months after initial treatment 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 - 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 |
Country | Name | City | State |
---|---|---|---|
Denmark | Aarhus University Hospital | Aarhus | |
Germany | University Hospital Eppendorf | Hamburg | |
Germany | University Medical Center | Mainz | |
Netherlands | Academic Medical Center | Amsterdam | |
Switzerland | University Hospital | Zürich |
Lead Sponsor | Collaborator |
---|---|
Universitätsklinikum Hamburg-Eppendorf | Aarhus University Hospital, Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA), Agaplesion Markus Krankenhaus, Johannes Gutenberg University Mainz, McGill Faculty of Medicine, University Hospital, Zürich |
Denmark, Germany, Netherlands, Switzerland,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | any reported GERD data | procedure to five years after treatment | ||
Other | duration of procedure | duration of procedure (minutes) | procedure | |
Other | in-hospital stay | in-hospital stay of patients (days) | procedure | |
Other | length of myotomy | length of myotomy (centimeters) | procedure | |
Other | procedure related complications | any complication during performance of treatment that required conversion to either laparoscopic (POEM) or open surgical treatment | procedure | |
Primary | treatment success | treatment success is defined as an Eckardt Score =3 | 1 year after treatment | |
Secondary | procedure related adverse events | retrospective data for this timepoint can be used of the interval 2-8 months after the initial procedure | 3 months after treatment | |
Secondary | lower esophageal sphincter pressure (LESP) | retrospective data for this timepoint can be used of the interval 2-8 months after the initial procedure | 3 months after treatment | |
Secondary | symptomatic reflux and use of antacid medication | retrospective data for this timepoint can be used of the interval 2-8 months after the initial procedure | 3 months after treatment | |
Secondary | procedure related adverse events | retrospective data for this timepoint can be used of the interval 9-15 months after the initial procedure | 12 months after treatment | |
Secondary | lower esophageal sphincter pressure (LESP) | retrospective data for this timepoint can be used of the interval 9-15 months after the initial procedure | 12 months after treatment | |
Secondary | symptomatic reflux and use of antacid medication | retrospective data for this timepoint can be used of the interval 9-15 months after the initial procedure | 12 months after treatment |