Evaluation of Irisin Levels in Adult Forearm Fracture Surgery Under Infraclavicular Block and General Anesthesia
Starting soon · Not applicable
Conditions studied: Inflamation, Healing, Angiogenesis
In brief
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.
Key facts
- Study ID
- NCT07324681
- Run by
- Ankara City Hospital Bilkent
- People needed
- 90
- Starts
- 2026-01-25
- Expected to finish
- 2026-05-05
- Last updated by the study team
- 2026-01-09
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adults aged 18 to 65 years
- Scheduled for elective forearm fracture surgery
- Planned to receive either general anesthesia or infraclavicular brachial plexus block
- American Society of Anesthesiologists (ASA) physical status I-III
- Able to provide written and verbal informed consent
You may not qualify if…
- Age <18 years or >65 years
- Emergency surgery
- Refusal or inability to provide informed consent
- ASA physical status IV or V
- Known bone diseases or metabolic bone disorders
- Multiple trauma or associated organ injury
- Inability to mobilize
- Morbid obesity (BMI >40 kg/m²)
- Renal failure
- Hepatic failure
- Neurological deficits or sequelae
- Contraindication or allergy to any anesthetic agents used in the study
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.