Endolumenal Partial Myotomy for the Treatment of Esophageal Achalasia
Recruitment status was Recruiting
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
Purpose
Achalasia is a primary esophageal motility disorder where the lower esophageal sphincter fails to relax in response to swallowing with no well understood underlying cause. Surgical myotomy represents an appropriate therapeutic option. The purpose of this study is to evaluate flexible endoscopic myotomy, a novel therapeutic approach to overcome the need for invasive surgery.
| Condition | Intervention | Phase |
|---|---|---|
|
Achalasia |
Procedure: Per oral endolumenal myotomy |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Endpoint Classification: Safety/Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Endoscopic Submucosal Tunnel Dissection for Endolumenal Partial Myotomy of the Lower Esophageal Sphincter for Achalasia |
- Esophageal function testing [ Time Frame: 6 months ] [ Designated as safety issue: No ]esophageal manometry test, pH test, upper endoscopy,barium swallow
- Quality of life score [ Time Frame: 6 months ] [ Designated as safety issue: No ]quality of life questionaire
| Estimated Enrollment: | 20 |
| Study Start Date: | October 2010 |
| Estimated Primary Completion Date: | October 2012 (Final data collection date for primary outcome measure) |
-
Procedure: Per oral endolumenal myotomy
In this study, the investigators propose the use of a recent endolumenal technique for partial myotomy in patients suffering from esophageal achalasia.
Under general anesthesia patients will have upper endoscopy. Submucosal injection and mucosal incision is created for entry into the submucosal space. A submucosal tunnel is then created using a needle knife or blunt dissection as appropriate. Dissection will continue distally beyond the lower esophageal sphincter. The inner circular muscle fibers will then be divided to achieve an adequate myotomy length. The mucosal entry is then closed appropriately.
Results will be compared to historical data of conventional Heller myotomies.
Eligibility| Ages Eligible for Study: | 18 Years to 85 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Candidate for elective Heller myotomy
- Ability to undergo general anesthesia
- Ability to give informed consent
Exclusion Criteria:
- Previous mediastinal or esophageal surgery
- Contraindications for EGD
Contacts and Locations| Contact: Lee L Swanstrom, MD | 503 281 0561 | lswanstrom@aol.com |
| United States, Oregon | |
| Good Samaritan Hospital, Legacy Health System | Recruiting |
| Portland, Oregon, United States, 97210 | |
| Contact: Lee L Swanstrom, MD 503-281-0561 lswanstrom@aol.com | |
| Sub-Investigator: Christy M Dunst, MD | |
| Sub-Investigator: Erwin Rieder, MD | |
| Sub-Investigator: Angi Gill, RN | |
More Information
Publications:
| Responsible Party: | Lee L. Swanstrom, MD, The Oregon Clinic |
| ClinicalTrials.gov Identifier: | NCT01302288 History of Changes |
| Other Study ID Numbers: | LEG1056 |
| Study First Received: | February 23, 2011 |
| Last Updated: | February 25, 2011 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by The Oregon Clinic:
|
endolumenal myotomy, per oral endoscopic myotomy |
Additional relevant MeSH terms:
|
Esophageal Achalasia Esophageal Motility Disorders Deglutition Disorders |
Esophageal Diseases Gastrointestinal Diseases Digestive System Diseases |
ClinicalTrials.gov processed this record on June 18, 2013