Endoscopic Treatment of Intestinal Fistulas and Perforations
Primary Purpose
Gastric Fistula
Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
gastro-gastric fistula closure
Sponsored by
About this trial
This is an interventional treatment trial for Gastric Fistula focused on measuring gastric fistula, perforation, endoscopy, closure, endolumenal
Eligibility Criteria
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
Sites / Locations
- Good Samaritan Hospital, Legacy Health System
Outcomes
Primary Outcome Measures
fistula or perforation closure possible; yes or no
Secondary Outcome Measures
fistula stays closed after 6 months
quality of life comparison, pre-op and after 6 months post-op
Full Information
NCT ID
NCT00835458
First Posted
February 2, 2009
Last Updated
February 10, 2009
Sponsor
Legacy Health System
Collaborators
Ethicon Endo-Surgery
1. Study Identification
Unique Protocol Identification Number
NCT00835458
Brief Title
Endoscopic Treatment of Intestinal Fistulas and Perforations
Official Title
Closure of Fistulas and Perforations Endoscopically to Avoid Laparoscopic or Open Surgery
Study Type
Interventional
2. Study Status
Record Verification Date
February 2009
Overall Recruitment Status
Unknown status
Study Start Date
February 2009 (undefined)
Primary Completion Date
October 2009 (Anticipated)
Study Completion Date
December 2010 (Anticipated)
3. Sponsor/Collaborators
Name of the Sponsor
Legacy Health System
Collaborators
Ethicon Endo-Surgery
4. Oversight
Data Monitoring Committee
No
5. 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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastric Fistula
Keywords
gastric fistula, perforation, endoscopy, closure, endolumenal
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
5 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Procedure
Intervention Name(s)
gastro-gastric fistula closure
Other Intervention Name(s)
Tissue Apposition System, TAS, 510(k) approval # K070151
Intervention Description
The mucosa surrounding the orifice of the fistula will be ablated using standard endoscopic techniques. Remnants of mucosa will be treated with argon-plasma coagulation. The mucosa free orifice of the fistula will be closed using the Tissue Apposition System. Tissue anchors with attached threads will be deployed through the intestinal wall full thickness using delivery needles through the working channel of the endoscope. After two anchors are deployed on both sides of the fistulas' orifice a knotting element will be cinched down to approximate the two sides of the fistulas' orifice. The procedure will be repeated until the fistulas' orifice is securely closed.
Primary Outcome Measure Information:
Title
fistula or perforation closure possible; yes or no
Time Frame
day of surgery
Secondary Outcome Measure Information:
Title
fistula stays closed after 6 months
Time Frame
6 months
Title
quality of life comparison, pre-op and after 6 months post-op
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lee L Swanstrom, MD, FACS
Organizational Affiliation
Legacy Health System
Official's Role
Principal Investigator
Facility Information:
Facility Name
Good Samaritan Hospital, Legacy Health System
City
Portland
State/Province
Oregon
ZIP/Postal Code
97210
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
17185093
Citation
Sumiyama K, Gostout CJ, Rajan E, Bakken TA, Deters JL, Knipschield MA. Endoscopic full-thickness closure of large gastric perforations by use of tissue anchors. Gastrointest Endosc. 2007 Jan;65(1):134-9. doi: 10.1016/j.gie.2006.01.050.
Results Reference
background
PubMed Identifier
18561931
Citation
Raju GS, Fritscher-Ravens A, Rothstein RI, Swain P, Gelrud A, Ahmed I, Gomez G, Winny M, Sonnanstine T, Bergstrom M, Park PO. Endoscopic closure of colon perforation compared to surgery in a porcine model: a randomized controlled trial (with videos). Gastrointest Endosc. 2008 Aug;68(2):324-32. doi: 10.1016/j.gie.2008.03.006. Epub 2008 Jun 17. Erratum In: Gastrointest Endosc. 2008 Sep;68(3):616.
Results Reference
background
PubMed Identifier
18609453
Citation
Sporn E, Miedema BW, Bachman SL, Astudillo JA, Loy TS, Calaluce R, Thaler K. Endoscopic colotomy closure after full thickness excision: comparison of T fastener with multiclip applier. Endoscopy. 2008 Jul;40(7):589-94. doi: 10.1055/s-2008-1077377.
Results Reference
background
PubMed Identifier
18294516
Citation
Bergstrom M, Swain P, Park PO. Early clinical experience with a new flexible endoscopic suturing method for natural orifice transluminal endoscopic surgery and intraluminal endosurgery (with videos). Gastrointest Endosc. 2008 Mar;67(3):528-33. doi: 10.1016/j.gie.2007.09.049.
Results Reference
background
Links:
URL
http://www.clinicaltrials.gov/ct2/show/NCT00553436
Description
Evaluation of an Endoscopic Suturing System for Tissue Apposition in Colonic Polypectomy
Learn more about this trial
Endoscopic Treatment of Intestinal Fistulas and Perforations
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