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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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17 October 2012 |
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Main ID: |
NCT01171612 |
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Date of registration:
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23/07/2010 |
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Primary sponsor: |
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Public title:
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Perioperative Management of Patients With Coronary Stents Undergoing Noncardiac Surgery
RegistStents |
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Scientific title:
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Evaluation and Monitoring of Perioperative Management of Patients With Coronary Stents Undergoing Noncardiac Surgery |
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Date of first enrolment:
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June 2009 |
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Target sample size:
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500 |
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Recruitment status: |
Recruiting |
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URL:
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http://clinicaltrials.gov/show/NCT01171612 |
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Study type:
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Observational |
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Study design:
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Observational Model: Cohort, Time Perspective: Prospective
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Countries of recruitment
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Spain
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Contacts
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Name:
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Anna Rodriguez-Pont |
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Address:
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Telephone:
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0034696485681 |
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Email:
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25836arp@comb.cat |
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Affiliation:
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Name:
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Anna Rodriguez-Pont, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Corporacio Sanitaria Parc Tauli |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- > 18 years old, with coronary stents
- ASA II-V
- noncardiac surgery wiht admission
- informed consent
Exclusion Criteria:
- < 18 years old
- ASA I
- ambulatory surgery
- pregnancy
- obstetric anaesthesia
- endoscopic procedures
- cardiac surgery
- not informed consent
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Acute Coronary Syndrome
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Coronary Stent Occlusion
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Surgery
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Primary Outcome(s)
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Major Adverse Cardiac Events (MACEs)
[Time Frame: up to 90 days after surgery]
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Secondary Outcome(s)
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Bleeding
[Time Frame: up to 30 days after surgery]
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Minor Cardiac Events
[Time Frame: up to 90 days after surgery]
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Neurovascular events.
[Time Frame: up to 90 days after surgery]
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Number of patients with adverse events related with Antiplatelet Therapy management
[Time Frame: 90 days after surgery]
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Secondary ID(s)
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CIR2009017
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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