Extended Peri-operative Tinzaparin to Improve Disease-free Survival in Patients With Resectable Colorectal Cancer

PHASE3CompletedINTERVENTIONAL
Enrollment

616

Participants

Timeline

Start Date

September 30, 2011

Primary Completion Date

December 31, 2020

Study Completion Date

February 1, 2021

Conditions
Adenocarcinoma of the Colon
Interventions
DRUG

Tinzaparin

The experimental arm will receive a subcutaneous injection of 4,500 IU of tinzaparin daily beginning at randomization and continued for 56 days following resection. There will be a minimum of one dose of pre-operative LMWH since it is not reasonable to delay surgery for the purpose of administering LMWH. The maximum duration of pre-operative LMWH will be 6 weeks.

DRUG

Tinzaparin

The control arm will receive a daily subcutaneous injection of 4,500 IU of tinzaparin beginning with the first post-operative dose and continued for the duration of hospitalization.

Trial Locations (16)

Unknown

Ghent University Hospital, Ghent

Health Sciences North, Greater Sudbury

Kingston General Hospital, Kingston

Montfort Hospital, Ottawa

Queensway Carleton Hospital, Ottawa

Sault Area Hospital, Sault Ste. Marie

Mount Sinai Hospital, Toronto

North York General Hospital, Toronto

St. Joseph's Health Centre, Toronto

Sunnybrook Health Science Centre, Toronto

Jewish General Hospital, Montreal

CHRU Brest, Brest

L8L 8E7

Hamilton Health Sciences Corporation, Hamilton

N6C 2R5

London Health Research Institute, London

K1H 8L6

The Ottawa Hospital, Ottawa

M3M 0B2

Humber River Hospital, Toronto

All Listed Sponsors
lead

Ottawa Hospital Research Institute

OTHER