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Early Ileostomy Closure for Rectal Cancer Patients in North America

Rectal Cancer | Ileostomy - Stoma

Our preliminary work demonstrates that there is buy-in from both patients and surgeons with regards to early ileostomy closure (EIC) for select rectal cancer patients undergoing restorative proctectomy (RP) and diverting loop ileostomy (DLI). The feedback from leaders in Europe further supports the need for a large scale randomized-controlled trial (RCT) on this subject in North America. Should the results of such a study be favourable, we believe it could support a change in practice that would be beneficial to patients and the health care system alike. Furthermore, our work will help identify which patients and practices are suitable for EIC.

The goal of our project is to determine whether EIC in rectal cancer patients undergoing RP with a DLI is safe, feasible and beneficial in a North American population. Specifically, our primary objective is to compare the severity of complications between patients undergoing EIC versus traditional (late) closure. Our secondary objectives include assessing the difference in quality of life (QoL), early and late bowel function, and cost of care between these two groups.

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Conditions de participation

  • Sexe:

    FEMALE

  • Âges admissibles:

    18 to 90

Critères de participation

Inclusion Criteria:

* Adult (≥18 years-old) patients
* Underwent restorative proctectomy by a laparoscopic, robotic, transanal total mesorectal excision, or open approach with creation of a diverting loop ileostomy for the treatment of rectal cancer
* Negative anastomotic "leak test" via CT scan with rectally-administered water-soluble contrast on post-operative day 7, 8 or 9.

Exclusion Criteria:

* Peri-operative immunosuppression (within 6 weeks of surgery date);
* Age-adjusted Charlson Comorbidity Index \>6;
* Other major surgery during the index operation;
* Any major complications (Clavien Dindo Grade III or greater) following restorative proctectomy;
* Inability to speak or comprehend English or French and inability to give informed consent.

Lieu de l'étude

London Health Sciences Centre
London Health Sciences Centre
London, Ontario
Canada

Contactez l'équipe d'étude

Primary Contact

Natasha Caminsky, MD

[email protected]
514-340-8222
Backup Contact

Nawar AlKhamesi, MD

[email protected]
St. Paul's Hospital, Providence Health Care
St. Paul's Hospital, Providence Health Care
Vancouver, British Columbia
Canada

Contactez l'équipe d'étude

Backup Contact

Amandeep Ghuman, MD, MPH, FRCSC

[email protected]
604-806-8860
Primary Contact

Natasha Caminsky, MD

[email protected]
514-340-8222
McGill University Health Centre
McGill University Health Centre
Montréal, Quebec
Canada

Contactez l'équipe d'étude

Primary Contact

Natasha Caminsky, MD

[email protected]
514-340-8222
Backup Contact

Marie Demian, MSc

[email protected]
Jewish General Hospital
Jewish General Hospital
Montreal, Quebec
Canada

Contactez l'équipe d'étude

Backup Contact

Natasha Caminsky, MD

[email protected]
Primary Contact

Sarah Sabboobeh, MSc

[email protected]
514-340-8222
Étude parrainée par
Jewish General Hospital
Participants recherchés
Plus d'informations
ID de l'étude: NCT05027737