RecruitingPhase 3NCT05168839

Intraoperative Indocyanine Green Fluorescence Angiography in Colorectal Surgery to Prevent Anastomotic Leakage

Intraoperative Indocyanine Green Fluorescence Angiography in Colorectal Surgery to Prevent Anastomotic Leakage: a Single-blind Phase III Multicenter Randomized Controlled Trial (Intergroup FRENCH-GRECCAR Trial)


Sponsor

Centre Hospitalier Universitaire de Besancon

Enrollment

1,010 participants

Start Date

Sep 26, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

Colorectal cancer (CRC) is the fourth most commonly diagnosed cancer in the world and the third in France. Its incidence is steadily rising in developing nations. Anastomotic leak (AL) is a major problem in colorectal surgery affecting at least 7% of patients operated on for left colonic cancer. It is the most feared complication after colorectal anastomosis, associated with mortality, prolonged hospitalization, impaired health related quality of life (HRQoL) and increased health care costs. Intraoperative fluorescence angiography (IOFA) with indocyanine green (ICG) may help preventing AL. Available studies on the effects of IOFA with ICG are heterogeneous and randomized controlled trial are scarce. Our aim is to demonstrate that IOFA with ICG could lead to a reduction of AL rate after left-sided or low anterior resection with anastomosis for CRC. The FLUOCOL-1 study is the first national, multicenter, single blind, randomized, 2-arm, phase III superiority clinical trial. The primary endpoint is the occurrence of an AL 90 days post-operation. AL is defined as any anastomotic dehiscence with leakage into the pelvic cavity diagnosed upon imaging or at surgical exploration or any isolated pelvic organ-space infection with no evidence of fistula as defined by the International Study Group of Rectal Cancer. The study population will be made of adult patients with left-sided or high rectal cancer scheduled to undergo elective left colectomy or high rectal resection (by open, laparoscopy or robotic surgery) and with expected stapled or hand-sewn intraperitoneal anastomosis. The exclusion criteria are mainly an emergent surgery; rectal cancer requiring total mesorectal excision and anastomosis expected below the peritoneal reflection; CRC requiring total or subtotal colectomy; CRC requiring transverse colectomy; recurrent CRC and locally advanced colorectal cancer requiring multi-visceral excision. A total of 1010 patients will be necessary (39 patients in each centre during 36 months). An interim analysis for efficacy and futility is scheduled when half of the participants will have been recruited. In case of positive results favoring IOFA, this study would define the use of IOFA as a standard of care in colorectal surgery. At the patient level, a significantly lower rate of AL will reduce hospital stay and stoma rate, and will ensure improved postoperative recovery, faster return to normal activity and better long-term oncologic outcomes.


Eligibility

Min Age: 18 Years

Inclusion Criteria4

  • Adult patients (age \>18 years)
  • Scheduled to undergo elective left colectomy or high rectal resection for cancer with intraperitoneal anastomosis.
  • Signed consent
  • Affiliated to the French social security system (CMU included).

Exclusion Criteria14

  • Emergent surgery.
  • Rectal cancer requiring total mesorectal excision and anastomosis below the peritoneal reflexion.
  • Colon cancer requiring total or subtotal colectomy defined as a right colectomy extended to the splenic flexure or more).
  • Colon cancer requiring transverse colectomy.
  • Recurrent colorectal cancer.
  • Locally advanced colorectal cancer requiring multi-visceral excision.
  • History of colectomy.
  • Associated concomitant resection of other organ (liver, etc.).
  • Previous pelvic radiotherapy for pathology unrelated to diagnosis with colon cancer e.g. treatment for prostate cancer.
  • Inflammatory bowel disease.
  • History of known allergy to indocyanine.
  • Pregnant patients.
  • Refusal to participate or inability to provide informed consent.
  • Protected adults (individuals under guardianship by court order).

Interventions

DRUGFLUO+ : Intraoperative fluorescence angiography (IOFA) with indocyanine green (ICG).

In the experimental arm (FLUO+), at least one 0.1mg/kg Infracyanine® bolus will be injected intravenously by the anesthesiologist. The detection of indocyanine green in the proximal colon segment will be done open or intracorporeally using a dedicated infrared camera. A surgical film describing the injection technique and fluorescence detection will be presented during the study set-up visits. An additional injection is allowed at the surgeon's discretion if necessary (change of anastomosis site). The time from injection to indocyanine green detection and any adverse events will be recorded.


Locations(32)

CHU de Toulouse

Toulouse, France

Clinique TIVOLI

Toulouse, France

Centre Hospitalier Universitaire Amiens-Picardie

Amiens, France

CH Annecy

Annecy, France

Centre Hospitalier Universitaire de Besançon

Besançon, France

Centre Hospitalier Bourgoin-Jallieu

Bourgoin, France

University Hospital of Dijon

Dijon, France

Centre Georges François Leclerc

Dijon, France

Centre Hospitalier Universitaire de Grenoble

La Tronche, France

Centre Hospitalier Universitaire de Lille

Lille, France

Centre lyonnais de chirurgie digestive

Lyon, France

Centre Hospitalier Lyon-Sud

Lyon, France

Hôpiatl Européen

Marseille, France

Hôpital La Timone

Marseille, France

Institut Paoli Calmettes

Marseille, France

Hôpital Nord AP-HM

Marseille, France

Hôpital St Joseph Marseille

Marseille, France

CHU de Nancy

Nancy, France

Hôpital Saint Louis

Paris, France

Hôpital Saint Antoine

Paris, France

Hôpital Cochin

Paris, France

Hôpital Bicêtre

Paris, France

Hôpital Européen Georges Pompidou

Paris, France

Centre Hospitalier de Pontoise

Pontoise, France

Hôpital Robert Debré

Reims, France

Ch Pontchaillou

Rennes, France

Centre Hospitalier Universitaire de Rouen

Rouen, France

Santé Atlantique

Saint-Herblain, France

Centre Hospitalier Universitaire de Strasbourg

Strasbourg, France

Centre Hospitalier de Tours

Tours, France

Institut cancérologie de Lorraine

Vandœuvre-lès-Nancy, France

Gustave Roussy

Villejuif, France

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT05168839


Related Trials