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Clinical Trials/EUCTR2007-006686-32-ES
EUCTR2007-006686-32-ES
Active, not recruiting
Not Applicable

Identificación de biomarcadores proteicos asociados a resistencia a la aspirina y a tienopiridinas en pacientes con cardiopatía isquémica establecida. (ESTUDIO BIRAT).Identification of new protein biomarkers associated with aspirin and thienopyridine resistance in stable coronary ischaemic patients: a proteomic study. (BIRAT Study). - BIRAT

FUNDACIÓN INVESTIGACIÓN BIOMEDICA DEL HOSPITAL CLINICO SAN CARLOS0 sitesMarch 27, 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
FUNDACIÓN INVESTIGACIÓN BIOMEDICA DEL HOSPITAL CLINICO SAN CARLOS
Status
Active, not recruiting
Last Updated
14 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 27, 2008
End Date
TBD
Last Updated
14 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
FUNDACIÓN INVESTIGACIÓN BIOMEDICA DEL HOSPITAL CLINICO SAN CARLOS

Eligibility Criteria

Inclusion Criteria

  • \-Men and women, ages 18 or older
  • \-Documented history of coronary disease define as \>50% stenosis in \>/\= 1 major coronary artery, clinically stable for at least 6 months.
  • \-Stable clinical situation at least during the last month.
  • \-Patients receiving AAS 100 mg daily at least during the last month and with the last AAS dosage 24 hours before
  • \-Written consent
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1\.2 Adults (18\-64 years) yes
  • F.1\.2\.1 Number of subjects for this age range
  • F.1\.3 Elderly (\>\=65 years) yes

Exclusion Criteria

  • \-Another antithrombotic treatment than AAS in the previous month
  • \-Presence of active infectious or tumoral disease
  • \-Recent trauma or major surgery, angioplasty or cathetherism during the last month
  • \-Atorvastatin treated patients
  • \-Patients receiving antiinflammatory treatment during the last month
  • \-No written consent

Outcomes

Primary Outcomes

Not specified

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