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Search / Trial NCT07014722

Contact Activation of Coagulation in Newly Inserted Central Venous Catheters

Launched by THOMAS KANDER · Jun 2, 2025

Trial Information

Current as of June 26, 2025

Not yet recruiting

Keywords

Coagulation Rotem Central Venous Catheter

ClinConnect Summary

This clinical trial is studying the effects of different types of central venous catheters (CVCs) on the body's blood clotting system. A CVC is a small plastic tube inserted into a large vein, usually in the neck or chest, that helps deliver medications and fluids and allows for blood sample collections. While CVCs are very useful, they can sometimes cause blood clots, which can lead to serious health issues. The goal of this study is to compare four commonly used CVCs to understand how each one affects blood clotting after they are inserted.

To be eligible for this trial, participants must be at least 18 years old and need a CVC for medical reasons. They should not be using blood-thinning medications, except for specific low-dose options. Participants will be randomly assigned to one of the four catheter types, and researchers will take two blood samples from the new catheter to see how it interacts with the blood. This study aims to gather important information that could help improve safety measures for patients using CVCs and reduce the risk of blood clots.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria
  • Participants must meet all of the following criteria to be included in the study:
  • Clinical indication for the placement of a two-lumen central venous catheter (length 150-160 mm).
  • Age ≥18 years. Signed informed consent.
  • No current use of anticoagulants or platelet inhibitors, except:
  • Prophylactic low molecular weight heparin (LMWH),
  • Double prophylactic dose of LMWH,
  • Acetylsalicylic acid (ASA).
  • Exclusion Criteria
  • Participants meeting any of the following criteria will be excluded:
  • Prothrombin complex (pK/INR) outside the normal range (0.9-1.2), if already available.
  • Platelet count \<140 × 10⁹/L, if already available.
  • Haemoglobin \< 80 g/L, if already available.
  • * Known coagulopathic conditions, including but not limited to:
  • Activated protein C (APC) resistance,
  • Hemophilia A or B,
  • Vitamin K deficiency,
  • Disseminated intravascular coagulation (DIC),
  • Antiphospholipid syndrome,
  • von Willebrand disease, Other known congenital or acquired bleeding disorders.

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.

Locations

Lund, Skåne, Sweden

Lund, , Sweden

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported