Endoscopic Mucosal Resection (EMR) for Diagnosis of Hirschsprung's Disease (EDGE)
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
Purpose
The purpose of this study is to compare the diagnostic yield with endoscopic mucosal resection (EMR) in hirschsprung's disease versus that of standard rectal suction biopsy. In order to compare EMR versus rectal suction biopsy, patients' diagnostic specimens will be analyzed by tissue size, the presence of submucosal tissue, and positive acteylcholinesterase staining. Additionally, the proportion of patients who would have required subsequent full thickness surgical biopsy with each technique will be compared. Biopsy results will be compared with clinical data including history, Bristol stool scale, anorectal manometry results and SITZ markers studies. Finally, the estimated costs that would have been incurred with each method will be evaluated.
| Condition | Intervention | Phase |
|---|---|---|
|
Chronic Constipation Hirschsprung's Disease |
Procedure: Endoscopic Mucosal Resection (EMR) |
Phase 1 Phase 2 |
| Study Type: | Interventional |
| Study Design: | Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Diagnostic |
| Official Title: | Endoscopic Mucosal Resection for the Diagnosis of a-Ganglionosis, a Controlled Prospective Trial |
- The major goal of this study is to test the hypothesis that EMR will result in a higher proportion of diagnostic specimens than RSB in patients sent for rectal suction biopsy. [ Time Frame: April 2009 ] [ Designated as safety issue: No ]
- Secondary outcome variables include the size of the specimen, the presence of ganglionic tissue, the presence of submucosal tissue, and the positivity of the acetylcholinesterase stain. [ Time Frame: April 2009 ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 50 |
| Study Start Date: | October 2007 |
| Estimated Study Completion Date: | April 2009 |
| Estimated Primary Completion Date: | April 2009 (Final data collection date for primary outcome measure) |
-
Procedure: Endoscopic Mucosal Resection (EMR)
Eligibility| Ages Eligible for Study: | 10 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Patients offered a rectal suction biopsy
Exclusion Criteria:
- any contraindication to general anesthesia or conscious sedation
- contraindication to endoscopy
- untreated or unmanageable coaguloapathy
- thrombocytopenia (<50)
- inability to provide informed consent.
Contacts and Locations| United States, Massachusetts | |
| Massachusetts General Hosptial | |
| Boston, Massachusetts, United States, 02114 | |
| Study Director: | Field F Willingham, MD, MPH | MGH |
| Study Director: | Garrett C Zella, MD | MGH |
| Study Director: | Mari Mino-Kenudson, MD | MGH |
| Principal Investigator: | Braden Kuo, MD | MGH |
| Study Director: | William R Brugge, MD, FASGE | MGH |
| Principal Investigator: | Leonel Rodriguez, MD | MGH |
| Study Director: | Clarissa Foy, NP | MGH |
More Information
No publications provided
| Responsible Party: | Leonel Rodriguez, MD, Massachusetts General Hosptial |
| ClinicalTrials.gov Identifier: | NCT00671684 History of Changes |
| Other Study ID Numbers: | 2007P001577 |
| Study First Received: | May 1, 2008 |
| Last Updated: | May 2, 2008 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Massachusetts General Hospital:
|
Hirschsprung's disease Constipation Endoscopy, digestive system Diagnosis Colonoscopy |
Additional relevant MeSH terms:
|
Constipation Hirschsprung Disease Signs and Symptoms, Digestive Signs and Symptoms Digestive System Abnormalities Digestive System Diseases |
Megacolon Colonic Diseases Intestinal Diseases Gastrointestinal Diseases Congenital Abnormalities |
ClinicalTrials.gov processed this record on May 21, 2013