Comparison of Myocardial Injury After Noncardiac Surgery (MINS) Incidence in Supine vs. Prone Positioning During Percutaneous Nephrolithotomy (PNL)

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age40+
SponsorMedipol University

About this trial

This prospective cohort study aims to compare the incidence of Myocardial Injury after Noncardiac Surgery (MINS) in patients undergoing percutaneous nephrolithotomy (PNL) for kidney stones in supine versus prone positioning. MINS is defined as an elevated postoperative troponin level (≥0.03 ng/mL) within 48 hours after surgery. Approximately 400 patients will be enrolled, with 200 patients in each positioning group (supine and prone). The primary outcome is the incidence of MINS, assessed through troponin measurements and electrocardiogram (ECG) findings. Secondary outcomes include intraoperative complications, duration of surgery, and postoperative recovery metrics. The study seeks to determine whether surgical positioning impacts MINS risk, potentially guiding safer surgical practices.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥40 years.

Patients undergoing percutaneous nephrolithotomy (PNL) for kidney stones.

Willing and able to provide informed consent.

Disqualifiers

Known coronary artery disease, heart failure, or other significant cardiovascular conditions.

Elevated preoperative troponin levels (≥0.03 ng/mL).

Major intraoperative complications (e.g., severe bleeding requiring transfusion).

Inability to comply with study procedures.

Trial design

Design model

Parallel

Treatments tested in this trial

  • blood sampling

    Diagnostic test

    measuring troponine preoperative and postoperative first and second day

Treatment groups

400 Participants
are divided into 2 treatment groups
Group A: Supine PNLOther 1 intervention
Group B: Prone PNLOther 1 intervention

Trial outcomes

Primary outcomes

1

Incidence of Myocardial Injury after Noncardiac Surgery (MINS)

Proportion of patients with postoperative troponin T levels ≥0.03 ng/mL within 48 hours after PNL, confirmed by ECG findings if ischemic changes are present.

Time frame
Up to 48 hours post-surgery

Secondary outcomes

1

Surgical Duration

Time from incision to closure (in minutes).

Time frame
During surgery.
2

Postoperative Hospital Stay

Duration of hospital stay after surgery (in days).

Time frame
From surgery to discharge.

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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Medipol University

Lead sponsor

Istanbul Medipol University Hospital

Collaborator

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