616
Participants
Start Date
September 30, 2011
Primary Completion Date
December 31, 2020
Study Completion Date
February 1, 2021
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.
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.
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
Hamilton Health Sciences Corporation, Hamilton
London Health Research Institute, London
The Ottawa Hospital, Ottawa
Humber River Hospital, Toronto
Lead Sponsor
Ottawa Hospital Research Institute
OTHER