Troponin-T for Detection of Perioperative Cardiovascular Events (VISION-pilot)
This study has been completed.
Sponsor:
Rigshospitalet, Denmark
Collaborator:
Copenhagen University Hospital at Herlev
Information provided by:
Rigshospitalet, Denmark
ClinicalTrials.gov Identifier:
NCT00443989
First received: March 6, 2007
Last updated: May 27, 2008
Last verified: March 2007
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Purpose
We will conduct a prospective cohort study evaluating the incidence of and optimal risk estimation model for major perioperative cardiovascular events in consecutive patients undergoing noncardiac surgery at the 'Herlev University Hospital'. This national pilot study in Denmark together with other national studies will inform the feasibility of a large prospective international cohort study.
| Condition |
|---|
|
Myocardial Infarction Cardiac Arrest |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | A Pilot for the:"Vascular Events In Noncardiac Surgery Patients Cohort Evaluation Study" |
Resource links provided by NLM:
Further study details as provided by Rigshospitalet, Denmark:
Biospecimen Retention: Samples Without DNA
Show Detailed Description
Troponin-T
| Enrollment: | 100 |
| Study Start Date: | March 2007 |
| Study Completion Date: | March 2008 |
| Primary Completion Date: | January 2008 (Final data collection date for primary outcome measure) |
Show Detailed Description
Eligibility| Ages Eligible for Study: | 45 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Study Population
Patients for major surgery more than 45 years of age
Criteria
Inclusion Criteria:
All patients undergoing noncardiac surgery are eligible if they:
- Are > 45 years of age
- Are undergoing noncardiac surgery requiring overnight hospital admission; AND
- Will receive a general or regional anesthetic
Exclusion Criteria:
- We will exclude patients who refuse 30 day or 6 month follow-up.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00443989
Locations
| Denmark | |
| Department of Anesthesiology and Intensive Care, Herlev University Hospital | |
| Herlev, Copenhagen, Denmark, DK-2730 | |
| Herlev Hospital | |
| Herlev, Copenhagen, Denmark, 2650 | |
Sponsors and Collaborators
Rigshospitalet, Denmark
Copenhagen University Hospital at Herlev
Investigators
| Principal Investigator: | Søren Borchorst, M.D. | University of Copenhagen |
More Information
No publications provided
| Responsible Party: | Jørn Wetterslev, Chief Physician, Copenhagen Trial Unit, Rigshospitalet, Copenhagen University Hospital, Denmark |
| ClinicalTrials.gov Identifier: | NCT00443989 History of Changes |
| Other Study ID Numbers: | H-KA-20060172 |
| Study First Received: | March 6, 2007 |
| Last Updated: | May 27, 2008 |
| Health Authority: | Denmark: Ethics Committee Denmark: Danish Dataprotection Agency |
Keywords provided by Rigshospitalet, Denmark:
|
Perioperative Myocardial Infarction Stroke Cardiac Death Cardiac Arrest |
Troponin-T Non-Cardiac surgery Death |
Additional relevant MeSH terms:
|
Heart Arrest Infarction Myocardial Infarction Heart Diseases Cardiovascular Diseases |
Ischemia Pathologic Processes Necrosis Myocardial Ischemia Vascular Diseases |
ClinicalTrials.gov processed this record on May 21, 2013