Clinical Trials Logo

Clinical Trial Summary

The investigators aim to assess tryptase test efficacy for measuring the allergic response to protamine during cardiac bypass surgery. Additionally, the investigators aim to establish a differential diagnosis on the basis of potential allergens or clinical causes.


Clinical Trial Description

Venous blood samples from cardiac surgery cases will be obtained for tryptase measurement upon admission to the operating room (OR) and immediately prior to and 30 min after protamine infusion initiation. A rapid effect-response-based clinical assessment will be made using clinical and laboratory monitoring data for diagnosis and treatment decisions during protamine infusion, which may complicate the recovery from surgery. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02644785
Study type Observational
Source Mustafa Kemal University
Contact
Status Completed
Phase N/A
Start date January 2016
Completion date February 2016

See also
  Status Clinical Trial Phase
Completed NCT03583567 - Effect of Anti-histamine in Prevention Systolic Hypotension After Protamine Phase 4
Not yet recruiting NCT06254404 - Impact of Protamine Dose Reduction on Platelet Aggregation After Extracorporeal Circulation for Minimally Invasive Aortic Valve Replacement Surgery N/A