About this trial
This randomized prospective study evaluates the effect of general anesthesia versus infraclavicular nerve block on perioperative serum irisin levels in adults undergoing forearm fracture surgery. Irisin levels will be measured preoperatively, at 30 minutes postoperatively, and at 24 hours postoperatively. The association between irisin changes and fracture healing will be explored as a secondary outcome.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Adults aged 18 to 65 years
Disqualifiers
Age <18 years or >65 years
Trial design
Parallel
Treatments tested in this trial
General Anesthesia (GA)
Procedure/SurgeryGeneral anesthesia administered according to institutional routine; anesthetic drugs and doses will be recorded.
Infraclavicular Brachial Plexus Blocks
Procedure/SurgeryUltrasound-guided infraclavicular block performed preoperatively; details of technique, local anesthetic drugs and doses will be recorded.
Treatment groups
Trial outcomes
Primary outcomes
Change in Serum Irisin Levels
Serum irisin levels (ng/dL) will be measured to evaluate the effect of anesthesia type on perioperative irisin response. Blood samples will be collected at three time points: preoperatively (baseline), 30 minutes postoperatively, and 24 hours postoperatively. Changes in irisin levels will be compared between the general anesthesia group and the infraclavicular block group.
Secondary outcomes
Radiological Fracture Healing and Callus Formation
Postoperative radiographs will be evaluated to assess fracture healing and callus formation. Radiological findings will be analyzed in relation to perioperative changes in serum irisin levels to explore a potential association between irisin response and fracture healing.
Locations
Sponsors and contacts
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