Evaluation of Irisin Levels in Adult Forearm Fracture Surgery Under Infraclavicular Block and General Anesthesia

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorAnkara City Hospital Bilkent

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 volunteers

Qualifiers

Adults aged 18 to 65 years

Disqualifiers

Age <18 years or >65 years

Trial design

Design model

Parallel

Treatments tested in this trial

  • General Anesthesia (GA)

    Procedure/Surgery

    General anesthesia administered according to institutional routine; anesthetic drugs and doses will be recorded.

  • Infraclavicular Brachial Plexus Blocks

    Procedure/Surgery

    Ultrasound-guided infraclavicular block performed preoperatively; details of technique, local anesthetic drugs and doses will be recorded.

Treatment groups

90 Participants
are divided into 2 treatment groups
Group A: General Anesthesia (GA) GroupActive comparator 1 intervention
Group B: Infraclavicular Block (ICB) GroupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

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.

Time frame
Preoperative (baseline), 30 minutes postoperatively, and 24 hours postoperatively

Secondary outcomes

1

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.

Time frame
Postoperative follow-up period (up to 6 months)

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: