Evaluating pain management techniques for hip surgery recovery
The Effect of Ultrasound-guided Pericapsular Nerve Block, Fascia Iliaca Compartment Block and Femoral Block on Postoperative Recovery Quality in Hip Surgery
This study is testing different pain relief methods after hip surgery to see which one helps older patients recover better and feel more comfortable.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 80 (estimated) |
| Ages | 18 Years to 85 Years |
| Sex | All |
| Sponsor | Antalya Training and Research Hospital Government |
| Locations | 1 site (Antalya) |
| Trial ID | NCT06389279 on ClinicalTrials.gov |
What this trial studies
This observational study aims to assess the impact of various ultrasound-guided nerve blocks, including the pericapsular nerve block, fascia iliaca compartment block, and femoral block, on the quality of recovery in patients undergoing hip surgery under spinal anesthesia. With a focus on multimodal analgesia, the study seeks to improve postoperative pain management and recovery outcomes for elderly patients who are particularly vulnerable to complications. The Quality of Recovery-15 (QoR-15) questionnaire will be utilized to evaluate patients' pain levels, physical comfort, independence, psychological support, and emotional status during the early postoperative period.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18-85 with elective hip fractures and an ASA classification of I-III.
Not a fit: Patients who are planned for general anesthesia or have multiple fractures, bleeding disorders, or contraindications for spinal anesthesia may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could significantly enhance postoperative recovery quality and pain management for patients undergoing hip surgery.
How similar studies have performed: Other studies have shown promising results with similar nerve block techniques in improving postoperative recovery, indicating that this approach is supported by existing evidence.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * elective hip fracture, * 18-85 years * American Society of Anaesthesiology (ASA) I-III Exclusion Criteria: * patients planned for general anesthesia * with multiple fractures * bleeding disorder * peripheral neuropathy * mental disorder * local anesthetic allergy * contraindications for spinal anesthesia (local infection, etc.) * declining to give written informed consent
Where this trial is running
Antalya
- University of Health Sciences, Antalya Training and Researh Hospital — Antalya, Turkey (Recruiting)
Study contacts
- Principal investigator: Arzu Karaveli, M.D. — University of Health Sciences, Antalya Training and Research Hospital
- Study coordinator: Arzu Karaveli
- Email: arzukaraveli@hotmail.com
- Phone: + 90 2422494400
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.