search
Back to results

A Randomized Comparison of Laparoscopic Myotomy and Pneumatic Dilatation for Achalasia

Primary Purpose

Esophageal Achalasia

Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
pneumatic dilatation
laparoscopic myotomy with partial fundoplication
Sponsored by
University Health Network, Toronto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Esophageal Achalasia focused on measuring laparoscopic myotomy, pneumatic dilatation, motility disorder, dysphasia, health-related quality of life

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Clinical diagnosis of achalasia by a physician manometric diagnosis of achalasia including both: Incomplete relaxation of the lower esophageal sphincter during swallowing (<80% of elevation over intragastric pressure and absence of esophageal peristalsis (peristalsis in <20% of initiated contractions) Facility with English, ability to complete English language questionnaires Exclusion Criteria: Pseudoachalasia: esophageal carcinoma; esophageal stricture; previous esophageal or gastric surgery; previous instrumentation of the lower esophageal sphincter i.e. suture, polymer injection, silicone band Previous gastric or esophageal surgery: fundoplication; Heller myotomy; gastric resection; vagotomy with or without gastric drainage Age 17 year or less Pregnancy Presence of severe comorbid illness: unstable angina; recent myocardial infarction (<6 months), cancer (except integumentary), unless free of disease for more than 5 years; end stage renal disease; previous stroke with cognitive, motor speech, or swallowing deficit persisting longer than one month; severe respiratory disease; cognitive impairment

Sites / Locations

  • St. Michael's Hospital, 30 Bond Street, Suite 16 048 Cardinal Carter Wing
  • University Health Network

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

1

2

Arm Description

pneumatic dilatation

Laparoscopic myotomy

Outcomes

Primary Outcome Measures

The achalasia severity questionnaire score at 1 year.

Secondary Outcome Measures

Generic health related quality of life (SF-36)
Gastrointestinal disease-specific quality of life (GIQLI)
Measures of esophageal physiology
Gastroesophageal reflux as measured by ambulatory 24-hr esophageal pH measurement
Clinical outcomes of care including short term outcomes, major complications, and long-term clinical outcomes.

Full Information

First Posted
September 9, 2005
Last Updated
May 20, 2014
Sponsor
University Health Network, Toronto
Collaborators
Canadian Institutes of Health Research (CIHR)
search

1. Study Identification

Unique Protocol Identification Number
NCT00188344
Brief Title
A Randomized Comparison of Laparoscopic Myotomy and Pneumatic Dilatation for Achalasia
Official Title
A Randomized Comparison of Laparoscopic Myotomy and Pneumatic Dilatation for Achalasia
Study Type
Interventional

2. Study Status

Record Verification Date
May 2014
Overall Recruitment Status
Unknown status
Study Start Date
September 2005 (undefined)
Primary Completion Date
March 2011 (Actual)
Study Completion Date
March 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Health Network, Toronto
Collaborators
Canadian Institutes of Health Research (CIHR)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to compare pneumatic dilatation and laparoscopic Heller myotomy in patients with achalasia in order to learn which of these two treatments should be recommended to patients in the future.
Detailed Description
Achalasia is a rare disease of the esophagus. It can cause difficulty swallowing, regurgitation of swallowed food, and chest pain. In achalasia, there are two problems in the esophagus. First, the esophagus does not properly push swallowed food down towards the stomach. Second, the valve at the lower end of the esophagus, called the lower esophageal sphincter, does not relax to allow food to pass from the esophagus into the stomach. Achalasia cannot be "cured". However, the symptoms of achalasia can be improved by treatment. Treatment is usually directed towards reducing the degree of blockage caused by the lower esophageal sphincter. the muscle of the lower esophageal sphincter can be stretched using a technique called pneumatic dilatation, or it can be divided (cut in half) during a surgical operation. The operation is called laparoscopic Heller myotomy, and is done by laparoscopic ("keyhole") surgery, where small incisions are used and patients usually stay in hospital 1-2 nights. Other treatments for achalasia, such as medications or injection of Botulinum Toxin Type A are not often used because they do not provide effective long-term improvement.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Esophageal Achalasia
Keywords
laparoscopic myotomy, pneumatic dilatation, motility disorder, dysphasia, health-related quality of life

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
56 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
pneumatic dilatation
Arm Title
2
Arm Type
Active Comparator
Arm Description
Laparoscopic myotomy
Intervention Type
Procedure
Intervention Name(s)
pneumatic dilatation
Intervention Description
The patient is on a liquid diet for 2 days prior to procedure. A sedative and pain killer by IV are given and the throat will be sprayed with local anesthetic. The gastroenterologist may perform an endoscopy prior to the dilatation to safely guide the dilator into position. A special dilator with a small balloon will be passed down the esophagus until it meets the stomach then the balloon will be inflated with air until the narrow part of the esophagus is opened. The patient will then be assessed for any perforation of the esophagus and monitored in the post-procedure unit for a few hours.
Intervention Type
Procedure
Intervention Name(s)
laparoscopic myotomy with partial fundoplication
Intervention Description
The abdomen is inflated with gas and cameras and instruments are inserted. The junction between the esophagus and stomach is identified. The muscle of the lower esophageal sphincter is divided. A portion of the stomach wall is secured to the lower esophagus. After surgery the patient is taken to the recovery room and when well enough moved to a ward. The patient may be discharged the following day.
Primary Outcome Measure Information:
Title
The achalasia severity questionnaire score at 1 year.
Time Frame
Baseline, M2, M6, Yrs 1 to 5
Secondary Outcome Measure Information:
Title
Generic health related quality of life (SF-36)
Time Frame
baseline, M2, M6, Yrs 1 to 5
Title
Gastrointestinal disease-specific quality of life (GIQLI)
Time Frame
baseline, M2, M6, Yrs 1 to 5
Title
Measures of esophageal physiology
Time Frame
baseline, M6
Title
Gastroesophageal reflux as measured by ambulatory 24-hr esophageal pH measurement
Time Frame
M6
Title
Clinical outcomes of care including short term outcomes, major complications, and long-term clinical outcomes.
Time Frame
Yrs 1 to 5

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Clinical diagnosis of achalasia by a physician manometric diagnosis of achalasia including both: Incomplete relaxation of the lower esophageal sphincter during swallowing (<80% of elevation over intragastric pressure and absence of esophageal peristalsis (peristalsis in <20% of initiated contractions) Facility with English, ability to complete English language questionnaires Exclusion Criteria: Pseudoachalasia: esophageal carcinoma; esophageal stricture; previous esophageal or gastric surgery; previous instrumentation of the lower esophageal sphincter i.e. suture, polymer injection, silicone band Previous gastric or esophageal surgery: fundoplication; Heller myotomy; gastric resection; vagotomy with or without gastric drainage Age 17 year or less Pregnancy Presence of severe comorbid illness: unstable angina; recent myocardial infarction (<6 months), cancer (except integumentary), unless free of disease for more than 5 years; end stage renal disease; previous stroke with cognitive, motor speech, or swallowing deficit persisting longer than one month; severe respiratory disease; cognitive impairment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David R Urbach, MD
Organizational Affiliation
University Health Network, Toronto
Official's Role
Principal Investigator
Facility Information:
Facility Name
St. Michael's Hospital, 30 Bond Street, Suite 16 048 Cardinal Carter Wing
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5B 1W8
Country
Canada
Facility Name
University Health Network
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 2C4
Country
Canada

12. IPD Sharing Statement

Learn more about this trial

A Randomized Comparison of Laparoscopic Myotomy and Pneumatic Dilatation for Achalasia

We'll reach out to this number within 24 hrs