Trials / Recruiting
RecruitingNCT07000539
Indocyanine Green Fluorescence Angiography (ICG-FA) in Revisional Bariatric Surgery
Prospective Single-center Diagnostic Parallel-group Study to Determine the Minimal Dose of Indocyanine Green to Observe Vascular Perfussion in Revisional Bariatric Surgery.
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 108 (estimated)
- Sponsor
- Instituto Mexicano del Seguro Social · Other Government
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study will compare different doses of a green fluorescent product that is administered during weight loss surgery in order to observe where blood vessels are located. There is uncertainty around the optimal dose of this product for patients with obesity, so this study will aim to study if the dose in the minimal range recommended by international guidelines is sufficient for most patients or if higher doses are needed with increasing body mass index.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIAGNOSTIC_TEST | Indocyanine Green Angiogram | Three different doses of indocyanin green will be compared (5 mg, 7.5 mg, and 10 mg). These doses are within the range of currently recommended doses by the International Society for Fluorescence Guided Surgery (ISFGS) for bariatric surgery. |
Timeline
- Start date
- 2025-05-06
- Primary completion
- 2026-12-01
- Completion
- 2026-12-31
- First posted
- 2025-06-03
- Last updated
- 2026-03-27
Locations
1 site across 1 country: Mexico
Source: ClinicalTrials.gov record NCT07000539. Inclusion in this directory is not an endorsement.