Post-POEM GERD in Patients Undergoing Conventional Versus Oblique Fibers Sparing Posterior Myotomy for Achalasia Cardia
- Conditions
- GERD
- Interventions
- Procedure: Per-oral endoscopic myotomy
- Registration Number
- NCT04229342
- Lead Sponsor
- Asian Institute of Gastroenterology, India
- 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.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 114
- 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
- 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,
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Oblique or sling fiber sparing group Per-oral endoscopic myotomy In the oblique or sling fiber group, only the circular muscle fibers will be severed selectively and the sling fibers will be spared Conventional Per-oral endoscopic myotomy 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.
- Primary Outcome Measures
Name Time Method Significant Reflux Esophagitis, Los Angeles grade (≥grade B) 8 weeks Assessment of reflux esophagitis will be done at 8 weeks post procedure using Los Angeles grading system (grade A to D)
- Secondary Outcome Measures
Name Time Method Clinical success using Eckardt Score (minimum:0, maximum: 12) 6 months 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
Reflux Symptoms, GERD HRQL score (minimum score: 0, maximum score: 50) 8-weeks The symptoms of gastroesophageal reflux will be evaluated using symptom scores.
Barium column height on Timed barium swallow; Success: >50% reduction in barium column height 2 months Timed barium swallow will be performed after POEM procedure and Esophageal emptying will be seen and compared with pre-POEM timed barium esophagogram
Gastroesophageal reflux with DeMeester score at 8-weeks: DeMeester score≥14.7 abnormal, <14.7: normal 8 weeks DeMeester scores will be calculated at 8 weeks after the POEM procedure
Esophageal manometry 8 weeks 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).
Clinical Success, Eckardt Score (minimum: 0, maximum: 12), Eckardt Score≤3: success, >3: failure 8 weeks Clinical success will be evaluated using Eckardt scores
Esophageal acid exposure, Acid exposure time>6 abnormal, <4: normal, 4-6: inconclusive 8 weeks 24-hour pH impedance study will be performed at 8-weeks and esophageal acid exposure will be calculated
Trial Locations
- Locations (1)
Asian institute of Gastroenterology/AIG Hospitals
🇮🇳Hyderabad, Telangana, India