Bleeding Events Before vs After Lowering Departmental Platelet Transfusion Trigger
Launched by THOMAS KANDER · Dec 17, 2023
Trial Information
Current as of July 22, 2025
Recruiting
Keywords
ClinConnect Summary
**Clinical Trial Summary: Lowering Platelet Transfusion Triggers for Central Venous Catheters**
This clinical trial is investigating whether it is safe to reduce the number of platelets required before placing a central venous catheter (a tube inserted into a large vein to give treatment) in patients with low platelet counts. Platelets are important for blood clotting, and patients with certain blood disorders often have lower counts, which increases their risk of bleeding. The study aims to compare bleeding events after lowering the platelet transfusion trigger from 50,000 to just 10,000 platelets per cubic millimeter. Researchers want to ensure that this change does not lead to severe bleeding complications.
To be eligible for this trial, participants must be 18 years or older and need a central venous catheter for treatment in a hematology ward. The study is currently recruiting participants who meet these criteria. Those who join can expect to undergo monitoring for bleeding events after their catheter is placed. This research is important because it could help improve the safety and effectiveness of care for patients with low platelet counts. If you or a loved one are considering participation, it’s a great opportunity to contribute to important medical research.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • ≥ 18 years of age
- • Indication for central venous catheter placement.
- • Patients admitted to a hematological ward at the current department
- Exclusion Criteria:
- • Death within 24h after insertion of CVC.
About Thomas Kander
Thomas Kander is an esteemed clinical trial sponsor dedicated to advancing medical research and innovation. With a strong focus on ethical practices and patient safety, Thomas Kander leads multi-phase clinical trials aimed at developing groundbreaking therapies across various therapeutic areas. The organization collaborates with leading research institutions and healthcare professionals to ensure rigorous study design, comprehensive data analysis, and adherence to regulatory standards. Committed to improving patient outcomes, Thomas Kander strives to contribute significantly to the evolving landscape of healthcare through its commitment to scientific excellence and collaboration.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Lund, Lunds Universitet, Sweden
Patients applied
Trial Officials
Thomas Kander, PhD
Principal Investigator
Region Skåne Sweden
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported