NCT07081009

Brief Summary

The aim of this study is to evaluate the incidence of myocardial injury after noncardiac surgery (MINS) in patients undergoing lumbar surgery, and to investigate the associated risk factors.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
180

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Oct 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 15, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

July 23, 2025

Completed
2 months until next milestone

Study Start

First participant enrolled

October 1, 2025

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 25, 2026

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

April 24, 2026

Completed
Last Updated

October 6, 2025

Status Verified

July 1, 2025

Enrollment Period

6 months

First QC Date

July 15, 2025

Last Update Submit

October 1, 2025

Conditions

MYOCARD INFARCTUSNon Cardiac SurgeryLumbar SurgeryAnesthesia

Keywords

Myocardial injurynoncardiac surgery

Outcome Measures

Primary Outcomes (1)

  • 1. Ischemia-related myocardial damage after noncardiac surgery

    Ischemia-related myocardial damage occurring within 30 days after noncardiac surgery

    After surgery 30 days

Secondary Outcomes (1)

  • 2. Causes of myocardial damage due to ischemia following noncardiac surgery

    30 days

Study Arms (2)

Mins positivity

Patients with high sensitive troponin positivity after surgery

Mins Negative

Patients with negative high sensitive troponin after surgery

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

A total of 180 patients aged 18 years and older who are scheduled to undergo elective lumbar stabilization will be included. Participants will be enrolled upon physician approval and informed consent.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ankara City Hospital Bilkent

Ankara, 06800, Turkey (Türkiye)

RECRUITING

Central Study Contacts

Mehmet Şahap

CONTACT

05336826254drsahap@gmail.com

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
270 Days
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
asist prof

Study Record Dates

First Submitted

July 15, 2025

First Posted

July 23, 2025

Study Start

October 1, 2025

Primary Completion

March 25, 2026

Study Completion

April 24, 2026

Last Updated

October 6, 2025

Record last verified: 2025-07

Data Sharing

IPD Sharing
Will not share

Due to the inadequate database network, patient information will not be shared with third parties. Patient data may be shared with journals upon request.

Locations

TU(1)