Clinical trial Recruiting at 1 site Observational Ages 18 and up

Detecting heart muscle injury during below-knee leg surgery with peripheral nerve block

Official title: Evaluation of Perioperative Myocardial Injury in Patients Undergoing Below-knee Lower Extremity Surgery With Peripheral Nerve Block

Run by Ankara City Hospital Bilkent · NCT07241572 · Data updated 2026-11-12

This will test whether measuring high‑sensitive troponin I during and after below‑knee leg surgery can detect heart muscle damage in adults receiving peripheral nerve blocks.

More Myocardial Ischemia trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment54 (estimated)
SponsorAnkara City Hospital Bilkent
Academic / other
Locations1 site (Ankara)
StatusRecruiting
StartedSeptember 1, 2025
Main results expectedDecember 31, 2025
Study endsJanuary 10, 2026
Registry record updatedDecember 1, 2025
Trial IDNCT07241572 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18 and older who are undergoing below‑knee lower extremity surgery with peripheral nerve block, are able to give informed consent, and meet ASA I–IV criteria are ideal candidates.

Probably not a fit

Patients who cannot receive regional anesthesia, who refuse participation, or whose care is not managed at the study site are not eligible and therefore will not benefit from this protocol.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is an observational study that measures high‑sensitive troponin I levels before surgery, during the operation, and at 24 and 48 hours after below‑knee lower extremity procedures performed with peripheral nerve blocks. Clinical and anesthetic details (type and dose of local anesthetic, intraoperative blood pressure, heart rate changes, inotrope use, fluids, urine output, and operation time) will be recorded to look for factors associated with troponin changes. The primary focus is whether perioperative troponin elevations indicate myocardial injury in this surgical setting; secondary analyses will explore which perioperative parameters correlate with troponin rise. All participants will have routine preoperative labs and hs‑troponin I measured as part of the monitoring protocol.

Why it matters

Potential benefit: If successful, this approach could identify otherwise unrecognized perioperative heart injury earlier in patients having below‑knee surgery, allowing clinicians to address cardiac risk sooner.

How similar studies have gone: High‑sensitive troponin is an established marker for perioperative myocardial injury in other surgical populations, but its routine monitoring during below‑knee procedures with peripheral nerve blocks is novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients over 18 years of age
* Patients undergoing below-knee lower extremity surgery
* Patients with ASA classifications I, II, III, and IV
* Patients who have consented before the procedure
* Patients who are literate and able to give consent

Exclusion Criteria:

* Patients in whom regional anesthesia is contraindicated
* Patients who refuse to participate in the study

Where it's running

  • Ankara Bilkent City Hospital
    Ankara, Turkey (Türkiye)
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.