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Clinical Trials/NCT01438398
NCT01438398
Completed
Not Applicable

A Prospective, Single Center, Proof of Concept Pilot Study of the Efficacy and Safety of Submucosal Endoscopic Myotomy With Mucosal Flap (SEMF) Technique in the Treatment of Patients With Achalasia

Winthrop University Hospital1 site in 1 country120 target enrollmentApril 8, 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Achalasia
Sponsor
Winthrop University Hospital
Enrollment
120
Locations
1
Primary Endpoint
Change in Lower esophageal sphincter pressure (LES)
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The purpose of this study is to learn about the safety and usefulness of a procedure called endoscopic submucosal myotomy, which is a new technique in the treatment of achalasia. Achalasia is a disorder involving the lack of smooth muscle relaxation and sustained high pressure in the sphincter (muscle) of the lower esophagus. This may result in symptoms such as difficulty in swallowing, chest pain, regurgitation of food and eventually, weight loss.

For more than a decade, a laparoscopic surgical procedure known as Heller myotomy has been the primary treatment for achalasia in patients with low surgical risk. In Heller myotomy, the surgeon makes three to four small abdominal incisions, inserts tube-like instruments through them, and once inside, the junction between the esophagus and stomach is found, a lengthwise incision is made on the muscular ring surrounding the lower esophageal sphincter which weakens the muscle and the lower esophageal sphincter or muscle (LES) is then able to open more easily. However, there is an emerging field known as natural orifice (opening) transluminal (through the lumen) endoscopic surgery (NOTES). This approach involves passing an endoscope - a thin tube with a built-in camera, light and minuscule tools through the natural opening in the body, like the mouth in order to perform less invasive surgery without any external wounds or scars. The procedure is done using the Submucosal Endoscopy with Mucosal Flap (SEMF) technique which involves passing an endoscope through the mouth into the esophagus, where a small incision is made on the lining of the esophagus, known as the mucosa. A balloon is then inserted and dilated in the submucosa - the layer between the inner lining of the esophagus and the outer wall consisting of the muscle of the esophagus. Dilation of the balloon in the submucosa creates a tunnel that allows insertion of the endoscope and access to the muscle of the lower esophageal sphincter (LES). A long incision is then carefully made on the posterior portion of the muscular ring that forms the LES. The incision divides the muscle fibers of the LES, which weakens the muscle, allowing for the easier passage of food while preserving some valve function to prevent reflux of acid from the stomach into the esophagus.

The expected duration of participation is up to 10 years from the time study participants undergo the endoscopic surgical procedure.

Detailed Description

The safety of the procedure and feasibility of the study will be measured by improvement in subjects' symptoms score, decrease in LES pressure, as well as the number and severity of complications or adverse events experienced by the subjects. A modified Eckhardt dysphagia assessment tool will be used in grading the dysphagia symptoms.

Registry
clinicaltrials.gov
Start Date
April 8, 2011
End Date
October 22, 2015
Last Updated
8 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Stavros Stavropoulos, MD

Advanced Endoscopist

Winthrop University Hospital

Eligibility Criteria

Inclusion Criteria

  • Patients 18 years or older, male or female, belonging to any race or ethnic origin
  • Patients with manometric positive diagnosis of achalasia, with corresponding symptoms of dysphagia, regurgitation of food or chest pain
  • Patients who are willing and competent to sign Informed Consent and to comply with study related visits and procedures

Exclusion Criteria

  • Patients who are below 18 years of age
  • Presence of coagulopathy
  • Patients who, in the investigator's opinion, are medically unstable, are unable to give informed consent, or whose risks outweigh the benefits of participating in the study
  • Vulnerable subjects: Prisoners, persons with decisional incapacity, and any person who are directly involved in the study, including their immediate family members, and anybody who may have any conflict of interest such as employees of ERBE, USA.

Outcomes

Primary Outcomes

Change in Lower esophageal sphincter pressure (LES)

Time Frame: at 3 months post endoscopic myotomy

High Resolution Esophageal Manometry will be done at 3 months to measure LES and the result will be compared to baseline or pre-endoscopic myotomy LES pressure.

Change in frequency of dysphagia

Time Frame: 4 weeks post procedure

Swallowing difficulty (dysphagia) will be assessed using the Modified Eckhardt Dysphagia Assessment Tool which includes asking the patient how often he/she experiences swallowing difficulty (0 = none, 1 = occasional, 2 = daily, and 3 = every meal. The score will be compared to pre-myotomy score.

Change in frequency of Regurgitation

Time Frame: 4 weeks post procedure

Patient will be asked how often he/she brings up swallowed liquid/solid food or regurgitates (0 = none, 1 = occasional, 2 = daily, and 3 = every meal. The score will be compared to the score prior to the procedure.

Change in frequency of chest pain

Time Frame: 4 weeks post procedure

The patient will be asked how often he/she experiences chest pain and the frequency (0 = none, 1 = occasional, 2 = daily, and 3 = every meal. The score will be compared to pre-myotomy score.

Presence of perforation

Time Frame: During endoscopic myotomy procedure

Presence of perforation that is seen during the endoscopic procedure.

Presence of bleeding

Time Frame: During endoscopic myotomy procedure

Occurence of bleeding during the procedure.

Presence of mediastinal emphysema

Time Frame: During endoscopic myotomy procedure

Presence of mediastinal emphysema will be recorded.

Presence of Infection

Time Frame: 4 weeks post procedure

Presence of infection within the first 4 weeks post myotomy will be recorded.

Development of stricture at the myotomy site.

Time Frame: 3 months post procedure

Development of stricture will be assessed by performing an upper endoscopy for patients with change in their Modified Dysphagia Score.

Secondary Outcomes

  • Frequency of use of antacids (PPI, H-2 antagonists)(4 weeks post procedure)
  • Change in patient's weight(At 3, 6, 9, and 12 months post procedure.)
  • Presence and frequency of heartburn(4 weeks post procedure)

Study Sites (1)

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