Clinical Trials Directory

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.