Trials / Unknown
UnknownNCT00778492
Thrombelastogram in Patients Receiving Antiplatelet Medication Undergoing Cardiac Surgery
Thrombelastogram and Predicting Microvascular Bleeding in Patients Receiving Antiplatelet Medication Undergoing Cardiac Surgery
- Status
- Unknown
- Phase
- —
- Study type
- Observational
- Enrollment
- 60 (estimated)
- Sponsor
- Sheba Medical Center · Other Government
- Sex
- All
- Age
- 18 Years – 90 Years
- Healthy volunteers
- Not accepted
Summary
Study Objective is to correlate the results of preoperative platelet mapping derived from modified TEG with clinically significant postoperative bleeding and consumption of blood products.
Detailed description
Study Design: Prospective observational study with blinded assessment of study endpoint variables. Collection of information concerning study endpoints will be performed by the investigator blinded to the results of preoperative testing of platelet function. The information will be collected from 60 patients undergoing cardiac surgery in the Department of Cardiac Surgery of Sheba Medical Center. Study endpoints 1. Primary endpoint- resternotomy for bleeding after the surgery. 2. Secondary endpoints- chest tube output during first 24 hours after the surgery; consumption of blood products during first 3 postoperative days.
Conditions
Timeline
- Start date
- 2008-05-01
- Primary completion
- 2008-10-01
- Completion
- 2008-12-01
- First posted
- 2008-10-23
- Last updated
- 2008-10-23
Locations
1 site across 1 country: Israel
Source: ClinicalTrials.gov record NCT00778492. Inclusion in this directory is not an endorsement.