Pre- Vs. Postoperative Thromboprophylaxis in Pancreatic Surgery
Launched by HELSINKI UNIVERSITY CENTRAL HOSPITAL · Feb 8, 2022
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is exploring the best timing for starting a treatment called thromboprophylaxis, which helps prevent blood clots, in patients undergoing pancreatic surgery. There are two approaches being compared: starting the treatment before the surgery (preoperative) or after the surgery (postoperative). This is important because pancreatic surgery carries risks of both blood clots and bleeding, and doctors currently do not have a clear, agreed-upon guideline on when to start this treatment. The study aims to find out which approach is more effective and safer for patients.
To participate in this trial, patients must be between 18 and 75 years old and be scheduled for specific types of pancreatic surgeries—either a pancreaticoduodenectomy, total pancreatectomy, or a distal pancreatectomy due to suspected cancer. However, patients who have taken blood-thinning medications in the month before surgery, those needing emergency surgery, or those with certain allergies or health conditions cannot join. Participants will be randomly assigned to receive either preoperative or postoperative thromboprophylaxis and will be closely monitored throughout the process. This study is currently recruiting and aims to provide better guidelines for managing blood clots in pancreatic surgery patients.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • All patients undergoing either
- • 1. pancreaticoduodenectomy or total pancreatectomy (for any indication) or
- • 2. distal pancreatectomy for suspicion of cancer
- Exclusion Criteria:
- • 1. Patient on anticoagulative medication (heparin, low-molecular weight heparin, warfarin, direct oral anticoagulants) during the month (30 days) preceding surgery
- • 2. Emergency operation (e.g. for trauma, infection or pancreatitis)
- • 3. Age \< 18 years
- • 4. Allergy or other contraindication to planned low-molecular weight heparin
- • 5. Inability to give written informed consent
- • 6. Pancreatic resection not performed (removed from analyses after randomization)
About Helsinki University Central Hospital
Helsinki University Central Hospital (HUCH) is a leading academic medical institution in Finland, dedicated to advancing healthcare through innovative research and clinical excellence. As a pivotal sponsor of clinical trials, HUCH integrates cutting-edge medical practices with rigorous scientific inquiry, fostering collaborations between researchers, healthcare professionals, and patients. The hospital is committed to enhancing patient outcomes and contributing to the global body of medical knowledge by conducting high-quality, ethically sound clinical studies across a diverse range of therapeutic areas. With a strong emphasis on education and training, HUCH plays a vital role in shaping the next generation of healthcare leaders and researchers.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Toronto, Ontario, Canada
Oulu, , Finland
Helsinki, , Finland
Tampere, , Finland
Oslo, , Norway
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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