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Thrombophilia clinical trials

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NCT ID: NCT06153394 Not yet recruiting - Thrombosis Clinical Trials

Prolonged Hypercoagulability Following Major Liver Resection for Malignancy

PRIORITY
Start date: June 1, 2024
Phase: Phase 3
Study type: Interventional

This clinical trial will investigate the ability of thromboelastrogrpahy (TEG®) to detect hypercoagulability after liver surgery and will examine the effect of extended thromboprophylaxis (medical treatment to prevent the development of blood clots inside blood vessels) in patients undergoing liver surgery for cancer treatment. The liver plays a key role in regulating the process of blood clotting. As a result, blood clots are a major cause of complications and death following liver surgery. This is especially true in cancer patients who are at a higher risk of developing blood clots. Current methods for preventing clotting complications after liver surgery include conventional coagulation blood tests (CCTs) and anticoagulant drugs, such as low molecular weight heparins (LMWHs). Current LMWH treatment is prescribed for one month after surgery, but studies show that the risk of developing blood clots can last up to 3 months. Studies also show that CCTs may not be as effective in detecting clotting issues as more comprehensive testing systems, such as TEG. This study will randomize 50 participants to receive 90 days of thromboprophylaxis (using the LMWH Redesca) or the standard of care 30 days (using the LMWH Fragmin) after liver surgery. The medication will be given by injection, similar to a regular vaccine or an insulin injection. Participants will inject the medication every day, for 30 or 90 days, after surgery. Participants will also have their blood tested for clotting issues via TEG testing before surgery and on post-operative days 1,3,5,30 and 90. After surgery, participants will be monitored by their surgeon for clotting complications and 3 year disease-free survival.

NCT ID: NCT04219449 Not yet recruiting - Beta-Thalassemia Clinical Trials

Thrombophilia In Beta Thalassemia

Start date: May 7, 2024
Phase:
Study type: Observational

β-thalassemia disease is one of the most common congenital hemolytic anemia commonly found in the malarial belt areas including the Mediterranean, the Middle East, Africa, Southeast Asian countries, and China.

NCT ID: NCT01019655 Not yet recruiting - Clinical trials for Pregnancy and Thrombophilia

Heparin for Pregnant Women With Thrombophilia

Start date: January 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to investigate whether heparin is an effective treatment in pregnant women at risk for thrombosis and other pregnancy-associated complications.