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

StatusActive, Not Recruiting
PhasePhase 4
Started
View on ClinicalTrials.gov ↗

Record History

  1. Primary completion date: Jun 2025 to Jul 3, 2027 Trial status: Recruiting to Active, Not Recruiting · Completion date: Jun 2027 to Jul 3, 2027 · Site details revisedv6 Show 3 more changesShow less
    • Trial status: Recruiting to Active, Not Recruiting
    • Completion date: Jun 2027 to Jul 3, 2027
    • Site details revised
  2. Primary completion date: Dec 2024 to Jun 2025 Completion date: Dec 2026 to Jun 2027v5 Show 1 more changeShow less
    • Completion date: Dec 2026 to Jun 2027
  3. Enrollment target: 250 to 300 Primary completion date: Sep 2024 to Dec 2024 · Completion date: Jan 2026 to Dec 2026v4 Show 2 more changesShow less
    • Primary completion date: Sep 2024 to Dec 2024
    • Completion date: Jan 2026 to Dec 2026
  4. Primary completion date: Jan 2024 to Sep 2024v3
  5. Secondary endpoints: details revised at 2 of 2 entries Eligibility criteria shortened, about 2 wordsv2 Show 1 more changeShow less
    • Eligibility criteria shortened, about 2 words

    See this version in full on ClinicalTrials.gov ↗

  6. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT06002906
Lead Sponsor University Health Network, Toronto
Collaborators: Stryker Endoscopy
Conditions Ulcer, Gastric, Obesity, Morbid
Enrollment 300 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov