Venous Thromboembolism (VTE) Clinical Trials

Find Venous Thromboembolism (VTE) Clinical Trials Near You

Prediction and Prevention of Venous Thrombo-embolism(VTE) During Chemotherapy Using Serial Determination of Haemostasis Biomarkers.

Status: Recruiting
Location: See all (3) locations...
Study Type: Observational
SUMMARY

Cancer patients are at higher risk of getting a blood clot (known as venous thromboembolism (VTE)) especially during chemotherapy and some patients are more at risk than others. These clots can be prevented by using blood thinners (known as anticoagulants) but these are not suitable for everyone as they also carry a risk of bleeding. This study aims to identify which chemotherapy patients are most at risk of a blood clot and at what point in their treatment this is likely to happen. In this project biomarkers in the blood that are involved in blood clotting will be measured in cancer patients at four stages during chemotherapy to see how the biomarkers change during treatment. The blood samples for these tests are taken at the same time as the normal routine blood tests done before a chemotherapy cycle. Biomarker levels will be compared between those patients who subsequently get a VTE and those who do not get a VTE. This will help develop a biomarker based blood test to predict clots during chemotherapy. The biomarker based test will also be compared with other methods of predicting VTE in cancer patients which are currently in use. In the future, this blood test might be used to see if patients are at high risk of a clot during chemotherapy and provide a method to optimise the use of preventative anticoagulants in cancer patients during chemotherapy.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients with a diagnosis of ovarian, lung, gastric or pancreatic cancer scheduled to undergo a course of chemotherapy who are undergoing adjuvant or neoadjuvant chemotherapy, or who are undergoing chemotherapy for relapsed disease or patients receiving targeted therapy in combination with chemotherapy

• Patients who are over 18 years of age

• Patients who are able to give full and informed written consent

Locations
Other Locations
Ireland
Cork University Hospital
RECRUITING
Cork
Mater Misericordiae University Hospital
RECRUITING
Dublin
Trinity Cancer St. James Cancer Institute
RECRUITING
Dublin
Contact Information
Primary
Lucy A Norris, PhD
lnorris@tcd.ie
353-1-8972728
Backup
Mark P Ward, PhD
wardm6@tcd.ie
353-1-8961563
Time Frame
Start Date: 2025-10-01
Estimated Completion Date: 2029-09-01
Participants
Target number of participants: 380
Treatments
Cancer patients undergoing chemotherapy
Lung, ovarian and pancreatic cancer patients undergoing chemotherapy.
Related Therapeutic Areas
Sponsors
Collaborators: Mater Misericordiae University Hospital, Cork University Hospital
Leads: University of Dublin, Trinity College

This content was sourced from clinicaltrials.gov