Pain management techniques for hip surgery
Comparative Analysis of Educational Interventions and Anesthetic Techniques for Enhanced Spinal Anesthesia Quality in Fractured Neck of Femur: Femoral Nerve Block, Periarticular Nerve Group (PENG) Block, and Preoperative IV Fentanyl
This study is testing a new pain management technique for hip surgery to see if it can help older patients feel less pain and recover better than traditional methods.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 210 (estimated) |
| Ages | 55 Years to 69 Years |
| Sex | All |
| Sponsor | Aswan University Hospital Academic / other |
| Locations | 1 site (Cairo) |
| Trial ID | NCT06537323 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of a new regional anesthetic technique called the pericapsular nerve group (PENG) block, alongside traditional femoral nerve block and preoperative IV fentanyl, to manage postoperative pain in patients undergoing total hip arthroplasties. The PENG block aims to provide more complete analgesia while minimizing muscle weakness, which is a common side effect of traditional nerve blocks. The study focuses on patients aged 55 to 69 years who are undergoing surgery for degenerative hip disease or traumatic hip fractures, conditions prevalent in the elderly population. By utilizing ultrasound guidance for the nerve blocks, the study seeks to enhance pain management outcomes and improve recovery experiences for patients.
Who should consider this trial
Good fit: Ideal candidates for this study are patients aged 55 to 69 years scheduled for total hip arthroplasties due to degenerative hip disease or traumatic hip fractures.
Not a fit: Patients with known allergies to local anesthetics will not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve postoperative pain management and recovery for patients undergoing hip surgery.
How similar studies have performed: While the PENG block is a relatively new technique, similar regional anesthetic approaches have shown promise in improving postoperative pain management in other studies.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * The included patient should be between 55 to 69 years Exclusion Criteria: * known allergies to local anesthetics
Where this trial is running
Cairo
- Zaher — Cairo, Egypt (Recruiting)
Study contacts
- Study coordinator: tarek sayed hemida, md
- Email: tarek.said@aswu.edu.eg
- Phone: 00201007363190
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.