MYOCARD INFARCTUSNCT07081009
Myocardial Injury After Noncardiac Surgery (MINS) in Lumbar Surgery Patients
An observational study of MYOCARD INFARCTUS and Non Cardiac Surgery, run by Ankara City Hospital Bilkent at 1 site in Turkey (Türkiye).
Trial 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. Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- MYOCARD INFARCTUS, Non Cardiac Surgery, Lumbar Surgery
- How many people
- 180 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 1 Oct 2025to 24 Apr 2026
- How long will I take part?
- 270 Days
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
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.
Inclusion criteria Age ≥18 years Elective lumbar stabilization surgery
Exclusion criteria History of cardiac surgery Recent acute MI (<30 days) Chronic elevated troponin levels
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Turkey (Türkiye)1 site, 1 recruiting
- Recruiting
Ankara City Hospital Bilkent
Ankara, 06800
Mehmet ŞAHAP
About this study
Official title: Evaluation of the Incidence and Risk Factors of Myocardial Injury After Noncardiac Surgery (MINS) in Lumbar Surgery Patients
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.
- Conditions
- MYOCARD INFARCTUS, Non Cardiac Surgery, Lumbar Surgery, Anesthesia
- Keywords
- Myocardial injury, noncardiac surgery
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Mins positivity | Patients with high sensitive troponin positivity after surgery | |
| Mins Negative | Patients with negative high sensitive troponin after surgery |
What is being measured
The primary outcome is the main question the study is designed to answer.
1. Ischemia-related myocardial damage after noncardiac surgery
Ischemia-related myocardial damage occurring within 30 days after noncardiac surgery
Measured: After surgery 30 days
Secondary outcomes (1)
2. Causes of myocardial damage due to ischemia following noncardiac surgery
To identify risk factors for myocardial damage due to ischemia following noncardiac surgery.
Measured: 30 days
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted23 Jul 2025
- Study start1 Oct 2025
- Primary completion25 Mar 2026 (estimated)
- Study completion24 Apr 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for MYOCARD INFARCTUSStudies of the same condition, open and under way.
- More trials run by Ankara City Hospital BilkentThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 180 participants (estimated)
- Target duration
- 270 Days
Sponsor and investigators
- Lead sponsor
- Ankara City Hospital Bilkent
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Mehmet sahap, Ankara City Hospital Bilkent
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07081009
- Sponsor's protocol ID
- mıns and lumbar surgery
- Status last verified
- Jul 2025
- First submitted
- 15 Jul 2025
- Last updated
- 6 Oct 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: Due to the inadequate database network, patient information will not be shared with third parties. Patient data may be shared with journals upon request.
Study at a glance
From the registry record, last updated by the sponsor on 6 Oct 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Evaluation of the Incidence and Risk Factors of Myocardial Injury After Noncardiac Surgery (MINS) in Lumbar Surgery Patients
- ClinicalTrials.gov ID
- NCT07081009
- Acronym / sponsor ID
- mıns and lumbar surgery
- Conditions
- MYOCARD INFARCTUS, Non Cardiac Surgery, Lumbar Surgery, Anesthesia
- Keywords
- Myocardial injury, noncardiac surgery
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 180 participants (estimated)
- Lead sponsor
- Ankara City Hospital BilkentUniversity, hospital or other
- Study start
- 1 Oct 2025 (actual)
- Primary completion
- 25 Mar 2026 (estimated)
- Study completion
- 24 Apr 2026 (estimated)
- First posted
- 23 Jul 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 270 Days
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Mins positivity | – | –Patients with high sensitive troponin positivity after surgery |
| Mins Negative | – | –Patients with negative high sensitive troponin after surgery |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
1. Ischemia-related myocardial damage after noncardiac surgery
Time frame: After surgery 30 days
Ischemia-related myocardial damage occurring within 30 days after noncardiac surgery
1 secondary outcome
2. Causes of myocardial damage due to ischemia following noncardiac surgery
Time frame: 30 days
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 6 Oct 2025.
- Individual participant dataSharing planned: No. Due to the inadequate database network, patient information will not be shared with third parties. Patient data may be shared with journals upon request.
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of MYOCARD INFARCTUS and Non Cardiac Surgery, run by Ankara City Hospital Bilkent at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 6 Oct 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Mehmet Şahap (05336826254, drsahap@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
1. Ischemia-related myocardial damage after noncardiac surgery (time frame: After surgery 30 days). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Oct 2025.