EUCTR2020-005298-29-NL
Active, not recruiting
Phase 1
Monitoring the effect of oral anticoagulants during percutaneous coronary intervention - MEASURE trial
ConditionsAnticoagulation during percutaneous coronary interventionTherapeutic area: Diseases [C] - Cardiovascular Diseases [C14]
DrugsHeparin
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Anticoagulation during percutaneous coronary intervention
- Sponsor
- St. Antonius Hospital
- Enrollment
- 120
- Status
- Active, not recruiting
- Last Updated
- 5 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patient must meet all of the following criteria:
- •\-Male or female \= 18 years
- •\-Undergoing elective PCI
- •\-Loaded with P2Y12 inhibitors before PCI
- •\-Patients with signed informed 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 20
- •F.1\.3 Elderly (\>\=65 years) yes
Exclusion Criteria
- •Patients who fulfill the above mentioned inclusion criteria but who manifest any of the following exclusion criteria will not be eligible for the study:
- •\-Patients with hematologic, renal (estimated glomerular filtration rate \<45 ml/min/1\.73m2\), hepatic (liver enzymes \>2 times the upper limit of normal), inflammatory (CRP \>2 times the upper limit of normal) or neoplastic disorders
- •\-Patients using nonsteroidal anti\-inflammatory drugs, corticosteroids, or hormone replacement therapy
Outcomes
Primary Outcomes
Not specified
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