A Clinical Study of Per Oral Endoscopic Myotomy (POEM) in Patients Suffering From Achalasia (POEM)
Primary Purpose
Achalasia
Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Procedure: Per Oral Endoscopic Myotomy (POEM)
Sponsored by
About this trial
This is an interventional treatment trial for Achalasia focused on measuring Heller myotomy
Eligibility Criteria
Inclusion Criteria:
- Candidate for a Heller myotomy
- No contra-indication to general anesthesia
- Their age is ≥18 years and ≤80 years
- Able to give written consent
Exclusion Criteria:
- Previous intervention for achalasia: any of previous Heller myotomy, Botox injections, endoscopic myotomy
- Previous mediastinal surgery
- Any anatomical esophageal anomaly that in the opinion of the investigator may render the intervention more difficult, such as sigmoid esophagus on the pre-operative barium swallow or hiatal hernia > 2cm.
- Body mass index (BMI) > 40
- Any medical condition, which in the judgment of the Investigator and/or designee makes the subject a poor candidate for the investigational procedure
- Pregnant or lactating female (Women of child bearing potential must take a pregnancy test prior to surgery)
Sites / Locations
- St. Joseph's Healthcare
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
peroral endoscopic myotomy (POEM)
Arm Description
The Procedure: per oral endoscopic myotomy (POEM)will be performed on all patients in this single arm study.
Outcomes
Primary Outcome Measures
feasibility of the POEM procedure in achalasia
Patients will be consecutively evaluated on effectiveness of the endoluminal procedure by conducting standard diagnostics including postoperative gastrografin swallow. After 6 months standard esophagogastroduodenoscopy (EGD), high-resolution manometry and pH impedance will be done and a Quality of Life questionnaire will be filled out. Results will be compared to historical data of 40 conventional laparoscopic Heller myotomies.
Secondary Outcome Measures
complications
post-operative complications, intra-operative outcomes as well as the Eckardt's grading systems of symptom severity and reflux grading secondary to achalasia.
Full Information
NCT ID
NCT01692106
First Posted
September 19, 2012
Last Updated
September 22, 2015
Sponsor
McMaster University
1. Study Identification
Unique Protocol Identification Number
NCT01692106
Brief Title
A Clinical Study of Per Oral Endoscopic Myotomy (POEM) in Patients Suffering From Achalasia
Acronym
POEM
Official Title
A Clinical Study of Per Oral Endoscopic Myotomy (POEM) in Patients Suffering From Achalasia.
Study Type
Interventional
2. Study Status
Record Verification Date
September 2015
Overall Recruitment Status
Completed
Study Start Date
November 2012 (undefined)
Primary Completion Date
December 2014 (Actual)
Study Completion Date
December 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
McMaster University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study evaluates the feasibility of endoscopic myotomy for achalasia. In achalasia, there is loss of relaxation of the lower esophageal sphincter (LES), as well as a higher baseline pressure in the LES. The most widespread treatment for this disease and the one that has the best long term results involves cutting the muscle layers of the lower esophagus and on the neighbouring stomach without injurying the underlying mucosa or inner layer of the esophageal wall. This is done during a surgery through the abdomen either with a big incision or more recently with the keyhole technique. This surgery has various potential complications, one of which being making a hole through the mucosa or not extending the cut on the muscle long enough to obtain adequate relaxation of the sphincter. The per oral endoscopic myotomy (POEM) is a new intervention that is done also under general anesthesia in the operating room; however, it involves no skin incisions and all the procedure is done through a fiber optic camera. It involves making a cut in the inner layer of the esophagus and then with cautery cut the muscle fibers responsible of the blockage and finally closing the initial opening with clips. In this study we will investigate the feasibility of this intervention both from a technical aspect as well as a logistical perspective given the local operating room constraints.
Detailed Description
All patients will have routine pre-operative EGD, manometry, barium swallow, ph-metry. Equally all patients will undergo Eckardt's and grading systems of symptom severity before and after the intervention. The patients will have a gastro-graffin swallow in the first day after the surgery.
Procedure: Under general anesthesia upper endoscopy is performed using a standard single channel gastroscope. Submucosal injection with 10 ml saline with 1% methylen blue at the level of the mid esophagus is initially performed. A small longitudinal submucosal incision is created using a standard needle knife. For a sufficient entry point as well as submucosal tunnel, a dilating balloon is inserted submucosally via the created incision similar to the technique used in standard endoscopic submucosal dissection. The balloon is slightly inflated to allow sufficient entrance of the endoscope. The gastroscope is advanced into the submucosal space and the tunnel is created via needle knife or blunt dissection as appropriate. The tunnel is created distally and is stopped several centimeters beyond the lower esophageal sphincter (LES), which can easily be identified. Using flexible scissors, a triangle tip- or respectively an isolated tip-knife the clearly visible circular muscles are divided starting 4 cm above the LES extending 2 cm beyond the previously identified esophageal border. The longitudinal and serosal layers are left intact. Finally the mucosal entry is closed with standard endoscopic clips. Patients will receive standard postoperative care for surgical myotomy, including long-term follow-up.
If for any reason the endoscopic treatment is unable to be completed or infeasible, a standard laparoscopic treatment will be performed.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Achalasia
Keywords
Heller myotomy
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Actual)
8. Arms, Groups, and Interventions
Arm Title
peroral endoscopic myotomy (POEM)
Arm Type
Experimental
Arm Description
The Procedure: per oral endoscopic myotomy (POEM)will be performed on all patients in this single arm study.
Intervention Type
Procedure
Intervention Name(s)
Procedure: Per Oral Endoscopic Myotomy (POEM)
Intervention Description
lower esophageal sphincter muscle is sectioned through an unique endoscopic approach.
Primary Outcome Measure Information:
Title
feasibility of the POEM procedure in achalasia
Description
Patients will be consecutively evaluated on effectiveness of the endoluminal procedure by conducting standard diagnostics including postoperative gastrografin swallow. After 6 months standard esophagogastroduodenoscopy (EGD), high-resolution manometry and pH impedance will be done and a Quality of Life questionnaire will be filled out. Results will be compared to historical data of 40 conventional laparoscopic Heller myotomies.
Time Frame
1-6 months
Secondary Outcome Measure Information:
Title
complications
Description
post-operative complications, intra-operative outcomes as well as the Eckardt's grading systems of symptom severity and reflux grading secondary to achalasia.
Time Frame
1-6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Candidate for a Heller myotomy
No contra-indication to general anesthesia
Their age is ≥18 years and ≤80 years
Able to give written consent
Exclusion Criteria:
Previous intervention for achalasia: any of previous Heller myotomy, Botox injections, endoscopic myotomy
Previous mediastinal surgery
Any anatomical esophageal anomaly that in the opinion of the investigator may render the intervention more difficult, such as sigmoid esophagus on the pre-operative barium swallow or hiatal hernia > 2cm.
Body mass index (BMI) > 40
Any medical condition, which in the judgment of the Investigator and/or designee makes the subject a poor candidate for the investigational procedure
Pregnant or lactating female (Women of child bearing potential must take a pregnancy test prior to surgery)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dennis Hong, MD
Organizational Affiliation
St. Josephs' Healthcare Hamilton
Official's Role
Principal Investigator
Facility Information:
Facility Name
St. Joseph's Healthcare
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8N 4A6
Country
Canada
12. IPD Sharing Statement
Learn more about this trial
A Clinical Study of Per Oral Endoscopic Myotomy (POEM) in Patients Suffering From Achalasia
We'll reach out to this number within 24 hrs