Troponin levels in patients undergoing spinal surgery:prone versus supine position.

Not Applicable

Completed

• Conditions: troponin elevation; degenerative spine disorders undergoing a spinal surgical procedure; Surgery - Other surgery; Cardiovascular - Other cardiovascular diseases

• Registration Number: ACTRN12616000421437
• Lead Sponsor: The Townsville Hospital Neurosurgical Department

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-04-01
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Completed
• Sex: Male
• Target Recruitment: 90

Inclusion Criteria

All adult patients undergoing elective spinal surgery for degenerative conditions

Exclusion Criteria

Paediatric population, oncologic surgery, emergency surgery

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
serum troponin I level[Measurement taken prior to surgery, between zero and eight hours after surgery depending on clinician availability and between eight and twenty-four hours following surgery depending on clinician availability.]

Secondary Outcome Measures

Name	Time	Method
Mortality[Thirty-days post surgery];Any presentation to any public hospital with suspicion of a cardiovascular complaint. i.e requiring investigation with serum Troponin I levels, electrocardiogram and/or coronary angiogram. As identified on electronic medical record review.[thirty-days post surgery]