Endoscopic Treatment of Intestinal Fistulas and Perforations

Sponsor
Legacy Health System (Other)
Overall Status
Unknown status
CT.gov ID
NCT00835458
Collaborator
Ethicon Endo-Surgery (Industry)
5
1
21.9
0.2

Study Details

Study Description

Brief Summary

Background: T-shaped tissue anchors have promise to close incisions and perforations of the intestines securely. The closure of perforations, gastro-gastric, or intestinal fistulas usually requires invasive open or laparoscopic surgery under general anesthesia and can be complex surgeries due to their reoperative or inflammatory nature.

Objective: The proposed use of full thickness tissue anchors adds a new surgical aspect to the endoscopic treatment of fistulas and perforations by offering a robust suture like closure of defects. Instead of a 20 cm abdominal incision or 3 or 4 one centimeter incisions with the related postoperative morbidity an endoscopic technique is used which requires no postoperative limitation of activities.

Methods: In this study the investigators propose to use an endoscopic technique that eliminates the need for open or laparoscopic surgery and provides a more robust endoscopic repair than is possible with traditional endoscopic tools. Patients who are scheduled to undergo surgery for intestinal fistulas will be screened for study eligibility. Patients who are scheduled to undergo complex polypectomy, or submucosal dissection will be screened for study eligibility and informed about all possible therapies in case of an iatrogenic perforation (open - laparoscopic surgery, endoscopic clipping, endoscopic closure with tissue anchors). A commercially available flexible endoscope will be inserted through the mouth and the fistula or perforation will be closed using the Tissue Approximation System (Ethicon Endo Surgery, Cincinnati, OH).

The investigators will initially evaluate the potential benefit, risks and impact on the patient's quality of life of this modified surgical technique in 5 patients.

Expected results: The potential advantages to the patients entered into this study result from the avoidance of open or laparoscopic surgery with the related risks (bleeding, injury of organs, post operative wound infection, hernia), shorter hospital stay, reduced postoperative pain, earlier return to work, and cosmetic advantage.

Condition or Disease Intervention/Treatment Phase
  • Procedure: gastro-gastric fistula closure
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
5 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Closure of Fistulas and Perforations Endoscopically to Avoid Laparoscopic or Open Surgery
Study Start Date :
Feb 1, 2009
Anticipated Primary Completion Date :
Oct 1, 2009
Anticipated Study Completion Date :
Dec 1, 2010

Outcome Measures

Primary Outcome Measures

  1. fistula or perforation closure possible; yes or no [day of surgery]

Secondary Outcome Measures

  1. fistula stays closed after 6 months [6 months]

  2. quality of life comparison, pre-op and after 6 months post-op [6 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 85 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Ability to undergo general anesthesia

  • Age > 18 yrs. of age and < 85 yrs. of age

  • Ability to give informed consent

Exclusion Criteria:
  • Contraindicated for esophagogastroduodenoscopy (EGD)

  • Contraindicated for colonoscopy

  • BMI < 40

  • Presence of esophageal stricture

  • Altered gastric anatomy

  • Intraabdominal abscess or severe inflammation

  • Pregnancy

Contacts and Locations

Locations

Site City State Country Postal Code
1 Good Samaritan Hospital, Legacy Health System Portland Oregon United States 97210

Sponsors and Collaborators

  • Legacy Health System
  • Ethicon Endo-Surgery

Investigators

  • Principal Investigator: Lee L Swanstrom, MD, FACS, Legacy Health System

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00835458
Other Study ID Numbers:
  • IIS GRANT#25206
First Posted:
Feb 3, 2009
Last Update Posted:
Feb 11, 2009
Last Verified:
Feb 1, 2009
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 11, 2009