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Post-POEM GERD in Patients Undergoing Conventional Versus Oblique Fibers Sparing Posterior Myotomy for Achalasia Cardia (POEM)

Primary Purpose

GERD

Status
Unknown status
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
Per-oral endoscopic myotomy
Sponsored by
Asian Institute of Gastroenterology, India
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for GERD

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Patients with type 1 and 2 achalasia with Eckardt score >3 (0-12 scale achalasia).
  2. Patients with age 18-75 years.
  3. Patients who are treatment naïve or have a history of pneumatic balloon dilatation.
  4. Patients who are willing and able to comply with the study procedures and provide written informed consent form to participate in the study

Exclusion Criteria:

  1. Patients with type 3 achalasia cardia or any other esophageal motility disorder,
  2. Patients who have undergone previous surgery of the esophagus or stomach,
  3. Patients with active severe esophagitis,
  4. Patients with large lower esophageal diverticula,
  5. Patients with large ( > 3cm ) hiatal hernia,
  6. Patients with sigmoid oesophagus,

Sites / Locations

  • Asian institute of Gastroenterology/AIG Hospitals

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Conventional

Oblique or sling fiber sparing group

Arm Description

In the "conventional group", standard posterior myotomy will be performed and the sling or the oblique fibers will not be spared beyond the gastroesophageal junction.

In the oblique or sling fiber group, only the circular muscle fibers will be severed selectively and the sling fibers will be spared

Outcomes

Primary Outcome Measures

Significant Reflux Esophagitis, Los Angeles grade (≥grade B)
Assessment of reflux esophagitis will be done at 8 weeks post procedure using Los Angeles grading system (grade A to D)

Secondary Outcome Measures

Clinical Success, Eckardt Score (minimum: 0, maximum: 12), Eckardt Score≤3: success, >3: failure
Clinical success will be evaluated using Eckardt scores
Clinical success using Eckardt Score (minimum:0, maximum: 12)
Clinical success will be evaluated using Eckardt scores. Eckardt Score≤3 will be considered as clinical success and >3 will be considered as clinical failure
Esophageal manometry
Esophageal manometry will be performed at 8 weeks and Integrated relaxation pressure will be calculated and presented in mmHg 5. Change in IRP pressure by Manometry ( Assessed at pre procedure & 8 weeks).
Barium column height on Timed barium swallow; Success: >50% reduction in barium column height
Timed barium swallow will be performed after POEM procedure and Esophageal emptying will be seen and compared with pre-POEM timed barium esophagogram
Esophageal acid exposure, Acid exposure time>6 abnormal, <4: normal, 4-6: inconclusive
24-hour pH impedance study will be performed at 8-weeks and esophageal acid exposure will be calculated
Reflux Symptoms, GERD HRQL score (minimum score: 0, maximum score: 50)
The symptoms of gastroesophageal reflux will be evaluated using symptom scores.
Gastroesophageal reflux with DeMeester score at 8-weeks: DeMeester score≥14.7 abnormal, <14.7: normal
DeMeester scores will be calculated at 8 weeks after the POEM procedure

Full Information

First Posted
January 7, 2020
Last Updated
October 5, 2020
Sponsor
Asian Institute of Gastroenterology, India
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1. Study Identification

Unique Protocol Identification Number
NCT04229342
Brief Title
Post-POEM GERD in Patients Undergoing Conventional Versus Oblique Fibers Sparing Posterior Myotomy for Achalasia Cardia
Acronym
POEM
Official Title
Comparison of Gastroesophageal Reflux Between Conventional Versus Oblique Fibers Sparing Endoscopic Myotomy for Achalasia Cardia - A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2020
Overall Recruitment Status
Unknown status
Study Start Date
January 6, 2020 (Actual)
Primary Completion Date
July 16, 2020 (Actual)
Study Completion Date
October 6, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Asian Institute of Gastroenterology, India

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
In this study, we will evaluate the incidence of reflux esophagitis between two different techniques of posterior per-oral endoscopic myotomy (POEM) i.e. conventional POEM versus oblique/ sling fiber sparing POEM. This is a randomized trial where the patients with idiopathic achalasia will be randomized in two groups in 1:1 fashion into groups.
Detailed Description
In this randomized trial, patients with idiopathic achalasia will undergo POEM using two techniques as follows. In the first technique, a conventional posterior POEM will be performed where the sling or oblique fibers will not be spared during POEM. Sling or oblique fibers will be recognized using the configuration of fibers below the gastroesophaeal junction and by identifying the border between the sling fibers and the circular fibers which is formed by the penetrating vessels. In the second group (Oblique fiber group), the sling fibers will be selectively spared and only the circular fibers will be spared. The other steps of the POEM procedure will be the same as described in the standard technique of POEM. These include submucosal injection of saline mixed with indigo carmine dye, mucosal incision, submucosal tunneling using triangular knife in spray coagulation mode (Effect 2, Watts 50), myotomy extending upto 2-4 cm below the gastroesophageal junction and the closure of mucosal incision using endoclips. Post POEM management: All the patients will be kept nil per oral for about 24-hours after the procedure. A timed barium swallow will be performed the next day and oral liquids will be started. A soft puried diet will be started from day 3 onwards. Oral proton pump inhibitors (PPIs) equivalent to 40 mg of Pantoprazole per day will be prescribed to all the patients unless a contraindication exists. Follow-up: The first evaluation will be performed at 2-months after POEM. During this evaluation, the following parameters will be recorded: symptom relief, reflux symptoms, and esophageal acid exposure. PPIs will be stopped for 1-2 weeks prior to the evaluation of GERD. Subsequent evaluation will be at 6-months for reflux symptoms and symptoms of achalasia using Eckardt scores.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
GERD

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
114 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Conventional
Arm Type
Active Comparator
Arm Description
In the "conventional group", standard posterior myotomy will be performed and the sling or the oblique fibers will not be spared beyond the gastroesophageal junction.
Arm Title
Oblique or sling fiber sparing group
Arm Type
Experimental
Arm Description
In the oblique or sling fiber group, only the circular muscle fibers will be severed selectively and the sling fibers will be spared
Intervention Type
Procedure
Intervention Name(s)
Per-oral endoscopic myotomy
Intervention Description
Per-oral endoscopic myotomy (POEM) is an endoscopic modality for the management of achalasia cardia. In this study, we will evaluate the impact of two different techniques of posterior POEM on the incidence of gastroesophageal reflux disease (GERD). Posterior POEM will be performed using the standard technique. The myotomy beyond the GEJ will be different in the two groups. In one group, the sling fibers will not be spared from dissection and in the second group, the sling fibers will be selectively spared from myotomy.
Primary Outcome Measure Information:
Title
Significant Reflux Esophagitis, Los Angeles grade (≥grade B)
Description
Assessment of reflux esophagitis will be done at 8 weeks post procedure using Los Angeles grading system (grade A to D)
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Clinical Success, Eckardt Score (minimum: 0, maximum: 12), Eckardt Score≤3: success, >3: failure
Description
Clinical success will be evaluated using Eckardt scores
Time Frame
8 weeks
Title
Clinical success using Eckardt Score (minimum:0, maximum: 12)
Description
Clinical success will be evaluated using Eckardt scores. Eckardt Score≤3 will be considered as clinical success and >3 will be considered as clinical failure
Time Frame
6 months
Title
Esophageal manometry
Description
Esophageal manometry will be performed at 8 weeks and Integrated relaxation pressure will be calculated and presented in mmHg 5. Change in IRP pressure by Manometry ( Assessed at pre procedure & 8 weeks).
Time Frame
8 weeks
Title
Barium column height on Timed barium swallow; Success: >50% reduction in barium column height
Description
Timed barium swallow will be performed after POEM procedure and Esophageal emptying will be seen and compared with pre-POEM timed barium esophagogram
Time Frame
2 months
Title
Esophageal acid exposure, Acid exposure time>6 abnormal, <4: normal, 4-6: inconclusive
Description
24-hour pH impedance study will be performed at 8-weeks and esophageal acid exposure will be calculated
Time Frame
8 weeks
Title
Reflux Symptoms, GERD HRQL score (minimum score: 0, maximum score: 50)
Description
The symptoms of gastroesophageal reflux will be evaluated using symptom scores.
Time Frame
8-weeks
Title
Gastroesophageal reflux with DeMeester score at 8-weeks: DeMeester score≥14.7 abnormal, <14.7: normal
Description
DeMeester scores will be calculated at 8 weeks after the POEM procedure
Time Frame
8 weeks

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: Patients with type 1 and 2 achalasia with Eckardt score >3 (0-12 scale achalasia). Patients with age 18-75 years. Patients who are treatment naïve or have a history of pneumatic balloon dilatation. Patients who are willing and able to comply with the study procedures and provide written informed consent form to participate in the study Exclusion Criteria: Patients with type 3 achalasia cardia or any other esophageal motility disorder, Patients who have undergone previous surgery of the esophagus or stomach, Patients with active severe esophagitis, Patients with large lower esophageal diverticula, Patients with large ( > 3cm ) hiatal hernia, Patients with sigmoid oesophagus,
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dr. Vincy Chandran, MBBS,MD
Organizational Affiliation
Asian Institute of Gastroenterology Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Asian institute of Gastroenterology/AIG Hospitals
City
Hyderabad
State/Province
Telangana
ZIP/Postal Code
500082
Country
India

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Post-POEM GERD in Patients Undergoing Conventional Versus Oblique Fibers Sparing Posterior Myotomy for Achalasia Cardia

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