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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

TypeNameDescription
DIAGNOSTIC_TESTIndocyanine Green AngiogramThree 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.

Indocyanine Green Fluorescence Angiography (ICG-FA) in Revisional Bariatric Surgery (NCT07000539) · Clinical Trials Directory