Clinical Trials Directory

Trials / Completed

CompletedNCT02914795

Platelet Function in Resuscitated Patients

Status
Completed
Phase
Study type
Observational
Enrollment
99 (actual)
Sponsor
Medical University of Graz · Academic / Other
Sex
All
Age
18 Years – 99 Years
Healthy volunteers
Not accepted

Summary

Approx. 65% of resuscitated patients at the intensive care unit for internal medicine are due to myocardial infarction. Almost all patients are initially diagnosed and treated in the cath lab. Therapy usually consists of one or more stent implantations. After implantation of a coronary stent, dual platelet inhibition is necessary for 12 months. Insufficient platelet inhibition causes an pronounced increase in risk of stent thrombosis. Therefore, knowledge of the individual platelet function is valuable. Several factors potentially promote a delayed or reduced mode of action of platelet function inhibitors in resuscitated patients: 1. oral administration is impossible and medication needs to be administered via a gastric line. 2. gastric absorption is delayed after resuscitation 3. according to current guidelines patients are treated with therapeutic hypothermia. Including the time of rewarming cooling period is \~48h

Detailed description

Patients after successful resuscitation associated to a myocardial infarction will be included into the study the morning after the index event. Patients get dual platelet inhibition at the discretion of the interventionist. Patients are treated with therapeutic hypothermia according to the local Standard operating procedure for 24h and rewarming is performed within an additional 20h. Platelet function is measured every morning and Aspirin mediated as well as P2Y12 (purinergic G protein-coupled receptors-12)-inhibition mediated platelet function inhibition is recorded. All relevant clinical data including APACHE (Acute Physiology and Chronic Health Evaluation) and SOFA ( Sequential Organ Failure Assessment score) scores are collected. The degree of platelet inhibition over time (7 days) and differences between the three drugs tested will be evaluated by optical aggregometry and by using the commercial VerifyNow test system.

Conditions

Interventions

TypeNameDescription
OTHERdiagnostic analysis of platelet functionanalysis of platelet aggregation using optical measurements as well as the commercial VerifyNow technique

Timeline

Start date
2015-06-01
Primary completion
2016-07-01
Completion
2016-08-01
First posted
2016-09-26
Last updated
2020-12-03
Results posted
2020-12-03

Locations

1 site across 1 country: Austria

Source: ClinicalTrials.gov record NCT02914795. Inclusion in this directory is not an endorsement.