Prospective Study on the Feasibility and Results of POEM in Idiopathic Achalasia (POEM)
Primary Purpose
Achalasia
Status
Completed
Phase
Phase 2
Locations
Italy
Study Type
Interventional
Intervention
Hybrid Knife
Sponsored by
About this trial
This is an interventional treatment trial for Achalasia focused on measuring achalasia, per oral endoscopic myotoymy, endoscopy
Eligibility Criteria
Inclusion Criteria:
- Age 18 to 75 years
- Manometric diagnosis of achalasia
- Eckardt score more than 3
- Informed consent
Exclusion Criteria:
- Increased surgical risk for important comorbidities,
- Pseudoachalasia
- Mega-esophagus (more than 7 cm) and or sigmoid esophagus,
- Previous esophageal or gastric surgery (with the exception of gastric perforation)
- Inability of completing the questionnarie
- Inability to keep a commitment for follow-up
- Esophageal diverticulum
Sites / Locations
- Endoscopy Unit, Humanitas Research Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Achalasia
Arm Description
Patients (age 18-75 years old) with diagnosis of achalasia, without megaesophagus or colonic esophagus, will undergo POEM with the hybrid knife.
Outcomes
Primary Outcome Measures
Feasibility
Percentage of patients with successful POEM
Clinical Success
A reduction of 2 or more points in the Eckardt score, that determines a score of 3 or more in 24 months.
Secondary Outcome Measures
Quality of Life
Quality of life as measured by questionnaires (SF36 and l'EORTC QLQ-OES24) that will be administered to the patients at 3 and 12 months.
Adverse events
Post-operative adverse events (perforation, bleeding, infection, aspiration, etc)
Reflux disease
Reflux disase as diagnosed clinically (HRQL questionnarie) or by 24-hour pH-metry
Treatment failure
Percentages of patients in which other interventions for dysphagia are required after the first POEM.
Efficacy
Basal and post-treatment pressure of the lower esophageal sphincter, as measured by manometry and esophageal follow-through.
Full Information
NCT ID
NCT02259283
First Posted
September 29, 2014
Last Updated
October 3, 2014
Sponsor
Istituto Clinico Humanitas
1. Study Identification
Unique Protocol Identification Number
NCT02259283
Brief Title
Prospective Study on the Feasibility and Results of POEM in Idiopathic Achalasia
Acronym
POEM
Official Title
Prospective Study on the Feasibility and Results of the Treatment of Idiopathic Achalasia With the POEM (Per Oral Endoscopic Myotomy) Technique
Study Type
Interventional
2. Study Status
Record Verification Date
October 2014
Overall Recruitment Status
Completed
Study Start Date
December 2012 (undefined)
Primary Completion Date
June 2014 (Actual)
Study Completion Date
September 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Istituto Clinico Humanitas
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Treatment options for achalasia include endoscopic dilations and surgical myotomy. Recently the POEM (Per oral endoscopic myotoymy) technique has been described. Patients undergo myotomy under endoscopic control. It has advantage over endoscopic dilation since myotomy is performed, and has advantage over surgery because it is performed endoscopically, thus is less invasive. One potential disadvantage in respect to surgery may be that it may determine higher rates of post-operative reflux. The purpose of this study is to prospectively assess the feasibility of PEOM in our Center with the new hybrid knife, and clinical results at 1, 3 and 12 months.
This is a prospective, phase II study. Ten patients (age 18-75 years old) with diagnosis of achalasia, without megaesophagus or colonic esophagus, will be included for the POEM procedure.
This study will last about 2 years. The aim is the feasibility, security and success rate of POEM for achalasia. Patients will be followed for at least one year.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Achalasia
Keywords
achalasia, per oral endoscopic myotoymy, endoscopy
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Achalasia
Arm Type
Experimental
Arm Description
Patients (age 18-75 years old) with diagnosis of achalasia, without megaesophagus or colonic esophagus, will undergo POEM with the hybrid knife.
Intervention Type
Device
Intervention Name(s)
Hybrid Knife
Intervention Description
POEM (Per oral endoscopic myotoymy) technique performed with the hybrid knife which combines injection and cutting in the same device.
Primary Outcome Measure Information:
Title
Feasibility
Description
Percentage of patients with successful POEM
Time Frame
24 months
Title
Clinical Success
Description
A reduction of 2 or more points in the Eckardt score, that determines a score of 3 or more in 24 months.
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Quality of Life
Description
Quality of life as measured by questionnaires (SF36 and l'EORTC QLQ-OES24) that will be administered to the patients at 3 and 12 months.
Time Frame
24 months
Title
Adverse events
Description
Post-operative adverse events (perforation, bleeding, infection, aspiration, etc)
Time Frame
24 months
Title
Reflux disease
Description
Reflux disase as diagnosed clinically (HRQL questionnarie) or by 24-hour pH-metry
Time Frame
24 months
Title
Treatment failure
Description
Percentages of patients in which other interventions for dysphagia are required after the first POEM.
Time Frame
24 months
Title
Efficacy
Description
Basal and post-treatment pressure of the lower esophageal sphincter, as measured by manometry and esophageal follow-through.
Time Frame
24 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age 18 to 75 years
Manometric diagnosis of achalasia
Eckardt score more than 3
Informed consent
Exclusion Criteria:
Increased surgical risk for important comorbidities,
Pseudoachalasia
Mega-esophagus (more than 7 cm) and or sigmoid esophagus,
Previous esophageal or gastric surgery (with the exception of gastric perforation)
Inability of completing the questionnarie
Inability to keep a commitment for follow-up
Esophageal diverticulum
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alessandro Repici, MD
Organizational Affiliation
Istituto Clinico Humanitas
Official's Role
Principal Investigator
Facility Information:
Facility Name
Endoscopy Unit, Humanitas Research Hospital
City
Rozzano
State/Province
Milano
ZIP/Postal Code
20089
Country
Italy
12. IPD Sharing Statement
Citations:
PubMed Identifier
1451966
Citation
Eckardt VF, Aignherr C, Bernhard G. Predictors of outcome in patients with achalasia treated by pneumatic dilation. Gastroenterology. 1992 Dec;103(6):1732-8. doi: 10.1016/0016-5085(92)91428-7.
Results Reference
background
PubMed Identifier
20354937
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.
Results Reference
background
PubMed Identifier
22982946
Citation
Swanstrom LL, Kurian A, Dunst CM, Sharata A, Bhayani N, Rieder E. Long-term outcomes of an endoscopic myotomy for achalasia: the POEM procedure. Ann Surg. 2012 Oct;256(4):659-67. doi: 10.1097/SLA.0b013e31826b5212.
Results Reference
background
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Prospective Study on the Feasibility and Results of POEM in Idiopathic Achalasia
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