Overview

The Use of Indocyanine Green to Visualize Blood Flow to the Gastrojejunostomy During Bariatric Surgery.

Status:
Recruiting
Trial end date:
2026-01-01
Target enrollment:
0
Participant gender:
All
Summary
This is an interventional pilot study aimed to evaluate the use of NIF imaging as an intraoperative aid to assess the anastomotic blood flow to the gastric pouch and gastrojejunostomy during Roux-en-Y gastric bypass surgery and to determine its long-term impact on the rate of marginal ulceration, leaks and stricture.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University Health Network, Toronto
Collaborator:
Stryker Endoscopy
Criteria
Inclusion Criteria:

- Capacity to provide informed consent.

- Over the Age of 18.

- Eligible for bariatric surgery in Ontario and deemed an appropriate candidate for RYGB
surgery by the bariatric program.

- Commit to follow-up within the bariatric program, including behavioral and dietary
modifications designed to aid in sustained weight-loss.

- Treatment of marginal ulcer with the revisional surgery.

Exclusion Criteria:

- Not willing to participate in study

- Contraindication to, or not planned to undergo RYGB

- Known allergy to indocyanine green or Sodium Iodide

- Is participant pregnant or planning to get pregnant in next two years

- Ongoing substance abuse or active smoking

- Bleeding diathesis or Coagulopathy

- Unwilling to take PPI medication Post operatively