A Study of Near-Infrared Fluorescence Imaging With ICG During Reconstructive Gynecologic Surgery

Running, not enrolling · Not applicable

Conditions studied: Gynecologic Surgery

In brief

The objective of this study is to assess whether Near-Infrared Fluorescence/NIR Imaging perfusion alters intraoperative management of the flap or of the participant wound bed.

Key facts

Study ID

NCT05071976

Run by

Memorial Sloan Kettering Cancer Center

People needed

15

Starts

2021-09-24

Expected to finish

2026-10-24

Last updated by the study team

2025-10-31

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Women undergoing a pelvic reconstruction procedure after radical gynecologic surgery for any indication at MSK.
• Age ≥18 years.

You may not qualify if…

• Women with hepatic dysfunction as evidenced by elevated transaminases (two times the upper limit of normal).
• Women with a history of cirrhosis or other chronic liver disease.
• Women with a documented severe or life threatening allergy to iodine.
• Women with an allergy to ICG or severe allergy to iodinated contrast.
• Women undergoing any free flap (non-pedicled) reconstruction.

Where it is running

• Memorial Sloan Kettering Basking Ridge (Consent and Followup) — Basking Ridge, New Jersey, United States
• Memorial Sloan Kettering Monmouth (Consent and Followup) — Middletown, New Jersey, United States
• Memorial Sloan Kettering Bergen (Consent and Followup) — Montvale, New Jersey, United States
• Memorial Sloan Kettering Suffolk - Commack (Consent and Followup) — Commack, New York, United States
• Memorial Sloan Kettering Westchester (Consent and Followup) — Harrison, New York, United States
• Memorial Sloan Kettering Cancer Center — New York, New York, United States
• Memorial Sloan Kettering Nassau (Consent and Followup) — Rockville Centre, New York, United States

Full record on ClinicalTrials.gov

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