Evaluation of Perioperative Myocardial Injury in Patients Undergoing Below-Knee Lower Extremity Surgery
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorAnkara City Hospital Bilkent
About this trial
The aim of this observational study was to detect myocardial damage by monitoring high-sensitive troponin I levels in patients undergoing below-knee extremity surgery with peripheral nerve block.
The primary question it aims to answer is:
How effective are peroperative high-sensitive troponin I levels in predicting myocardial damage?
High-sensitive troponin I levels will be monitored intraoperatively and at 24 and 48 hours postoperatively.
Eligibility criteria
Qualifiers
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
Disqualifiers
Patients in whom regional anesthesia is contraindicated
Patients who refuse to participate in the study
Trial design
Treatments tested in this trial
- high sensitive Troponin I
Treatment groups
54 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov