Intervention to Improve Utilization of Extended Venous Thromboembolism Prophylaxis After Cancer Surgery
Launched by MEDICAL UNIVERSITY OF SOUTH CAROLINA · Jun 7, 2024
Trial Information
Current as of August 19, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying how to improve the use of medications that help prevent dangerous blood clots in patients who have had major cancer surgery. Blood clots can be a serious problem after surgery, but many patients don’t receive the recommended medications after leaving the hospital. The researchers want to find out if educating surgeons and patients about the risks of blood clots can lead to more people getting these important medications after surgery.
To participate in this study, patients must be undergoing specific types of cancer surgeries, such as removal of the stomach or bladder, and they cannot have certain conditions, like severe kidney disease. Participants will receive information about blood clot risks when they leave the hospital and will complete a questionnaire to help researchers understand their knowledge and adherence to the prescribed medications. This study aims to improve patient care by ensuring that those at risk of blood clots receive the right support and treatment after their surgery.
Gender
ALL
Eligibility criteria
- • SURGEON CLUSTER
- Inclusion Criteria:
- • Surgeons performing cancer surgery within the Medical University of South Carolina (MUSC) system will be identified. Patients undergoing surgery for included cancers in the three hospitals will be identified using inclusion/exclusion criteria as follows. "Abdominopelvic cancer surgery" includes esophagectomy, gastrectomy, pancreatectomy, small bowel resection, colectomy, proctectomy, cystectomy, nephrectomy and hysterectomy / oophorectomy performed for a diagnosis of cancer as identified by Current Procedural Terminology (CPT) code and International Classification of Diseases, Tenth Revision (ICD-10) diagnosis code.
- Exclusion Criteria:
- • We will exclude patients receiving preoperative therapeutic anticoagulation within 30 days preoperatively, patients initiating therapeutic anticoagulation postoperatively and patients with chronic kidney disease grade 3 or higher. Patients with postoperative length of stay 30 days or greater will be excluded as ePpx duration is for 30 days postoperative.
- • PATIENT SURVEY
- Inclusion Criteria:
- • Patients undergoing surgery for included cancers in the three hospitals will be identified using inclusion/exclusion criteria as follows. "Abdominopelvic cancer surgery" includes esophagectomy, gastrectomy, pancreatectomy, small bowel resection, colectomy, proctectomy, cystectomy, nephrectomy and hysterectomy / oophorectomy performed for a diagnosis of cancer as identified by Current Procedural Terminology (CPT) code and International Classification of Diseases, Tenth Revision (ICD-10) diagnosis code.
- Exclusion Criteria:
- • We will exclude patients receiving preoperative therapeutic anticoagulation within 30 days preoperatively, patients initiating therapeutic anticoagulation postoperatively and patients with chronic kidney disease grade 3 or higher. Patients with postoperative length of stay 30 days or greater will be excluded as extended pharmacologic venous thromboembolism duration is for 30 days postoperative.
- • Lack of survey response.
About Medical University Of South Carolina
The Medical University of South Carolina (MUSC) is a leading academic health center dedicated to advancing medical research and improving patient care through innovative clinical trials. With a strong emphasis on translational medicine, MUSC leverages its extensive resources and expertise to facilitate groundbreaking studies across various medical disciplines. The institution is committed to fostering collaboration among researchers, healthcare professionals, and patients, ensuring that cutting-edge discoveries translate into effective treatments. As a pioneer in health education and research, MUSC plays a vital role in shaping the future of medicine and enhancing health outcomes in the community and beyond.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Charleston, South Carolina, United States
Patients applied
Trial Officials
Thomas Curran, MD MPH
Principal Investigator
Medical University of South Carolina
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported