Incidence, Predictors and Validation of Risk Scores to Predict Myocardial Infarction After Noncardiac Vascular Surgery

• Sponsor: Centro Hospitalar De São João, E.P.E. (Other)
• Overall Status: Completed
• CT.gov ID: NCT04051749
• Collaborator: (none)
• Enrollment: 306
• Actual Duration (Months): 6.9

Study Details

Study Description

Brief Summary

Evaluate the incidence and predictors of post-operative mortality after noncardiac Vascular Surgery and compare the performance of existing risk scores.

Condition or Disease	Intervention/Treatment	Phase
Complication of Surgical or Medical Care	Procedure: Noncardiac Vascular Surgery

Study Design

• Study Type: Observational
• Actual Enrollment: 306 participants
• Observational Model: Cohort
• Time Perspective: Prospective
• Official Title: Incidence, Predictors and Validation of Risk Scores to Predict Myocardial Infarction After Noncardiac Vascular Surgery, a Cohort Prospective Study
• Actual Study Start Date: Jan 1, 2015
• Actual Primary Completion Date: Apr 30, 2015
• Actual Study Completion Date: Jul 31, 2015

Arms and Interventions

Arm	Intervention/Treatment
Patients submitted to VS	Procedure: Noncardiac Vascular Surgery; Noncardiac Vascular Surgery

Outcome Measures

Primary Outcome Measures

1. Major Cardiac Events [30-day]

Secondary Outcome Measures

1. Mortality [30-day]

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

Inclusion Criteria:

• Elective arterial Vascular Surgery

• Patients > 18 years

Exclusion Criteria:

• Urgent/Emergent Surgery

• Patients < 18 years

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

• Centro Hospitalar De São João, E.P.E.

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Pedro Reis, Principal Investigator, Centro Hospitalar De São João, E.P.E.
• ClinicalTrials.gov Identifier: NCT04051749
• Other Study ID Numbers: CES 04-15
• First Posted: Aug 9, 2019
• Last Update Posted: May 14, 2020
• Last Verified: May 1, 2020

• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No
• Additional relevant MeSH terms: Myocardial Infarction; Infarction

Study Results

No Results Posted as of May 14, 2020