Trials / Completed
CompletedNCT02285738
Anti-Platelet and Statin Therapy to Prevent Cancer-Associated Thrombosis
Anti-Platelet and Statin Therapy to Prevent Cancer-Associated Thrombosis: A Pilot Study
- Status
- Completed
- Phase
- EARLY_Phase 1
- Study type
- Interventional
- Enrollment
- 17 (actual)
- Sponsor
- Case Comprehensive Cancer Center · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This research study examines the safety and feasibility of aspirin with or without Simvastatin in solid tumor patients at risk for VTE (Venous Thromboembolism - or blood clots - in the arms, lets, lungs, or other part of the body). One-fifth of all thrombotic (clotting) events occur in patients that have cancer. Changes in sP-selectin will be used as a measure of efficacy. We have chosen sP-selectin as the primary marker because of its role in hemostasis, because it is predictive of thrombosis in cancer patients and because of promising preliminary data. We expect that sP-selectin levels will be elevated in patients before therapy with aspirin and/or statin, but that these levels will fall significantly during treatment, rise during the observation phase, and fall during the second study period. Patients who take part in the study have been diagnosed with a solid tumor cancer and are considered to be intermediate to high risk for VTE. The standard of care is to give chemotherapy for solid tumors and treat clots which develop using blood thinners.
Detailed description
Objectives Primary: To determine efficacy of aspirin with and without simvastatin in solid tumor patients at high- or intermediate-risk for VTE, in reducing markers of platelet activation, levels of inflammatory and angiogenic cytokines measured using high-throughput approaches, and clinical and investigational measures of hemostatic activation. Secondary: To determine safety and feasibility of aspirin with or without simvastatin in solid tumor patients at high- or intermediate-risk for VTE
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Aspirin | 81mg/day for 4 weeks |
| DRUG | Simvastatin | Daily dose of Simvastatin for 4 weeks |
| OTHER | Observation | participants will be observed for thrombotic evens for 4 weeks |
Timeline
- Start date
- 2014-12-30
- Primary completion
- 2017-07-17
- Completion
- 2018-10-01
- First posted
- 2014-11-07
- Last updated
- 2019-05-08
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT02285738. Inclusion in this directory is not an endorsement.