Comparing two pain relief techniques after hip surgery
Comparative Study Between Ultrasound-Guided Lumbar Erector Spinae Plane Block and Fascia Iliaca Compartment Block for Postoperative Analgesia After Total Hip Arthroplasty
This study is testing which of two pain relief methods works better for people recovering from hip surgery.
Quick facts
| Phase | Phase 4 |
|---|---|
| Study type | Interventional |
| Enrollment | 75 (estimated) |
| Ages | 30 Years to 75 Years |
| Sex | All |
| Sponsor | Tanta University Academic / other |
| Locations | 1 site (Tanta, Elgharbia) |
| Trial ID | NCT05905510 on ClinicalTrials.gov |
What this trial studies
This study compares the effectiveness of two regional anesthesia techniques, the lumbar erector spinae plane block (L-ESPB) and the fascia iliaca compartment block (FICB), in providing pain relief for patients undergoing total hip arthroplasty. Using ultrasound guidance, the researchers will administer local anesthetics to assess which method offers better analgesia post-surgery. The study aims to improve postoperative pain management and enhance recovery for patients undergoing hip surgery.
Who should consider this trial
Good fit: Ideal candidates are patients aged 30-75 years, of both sexes, classified as ASA I-III, scheduled for unilateral hip surgery under spinal anesthesia.
Not a fit: Patients with a history of allergy to local anesthetics, those with certain medical conditions, or those who are unable to cooperate with researchers may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management strategies for patients undergoing total hip arthroplasty.
How similar studies have performed: Other studies have shown promising results with similar regional anesthesia techniques, indicating potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Patients aged 30-75 years from both sexes. 2. ASA I-III scheduled for unilateral hip surgery under spinal anesthesia. Exclusion Criteria: 1. Patients' refusal. 2. Patients who were unable to co-operate with researchers. 3. History of allergy to local anesthetics. 4. Local infection at the site of the block. 5. Patients with bleeding and coagulation disorders. 6. Patients with renal, hepatic, cardiac decompensation, or spine deformities. 7. Patients receiving opioids for chronic analgesic therapy 8. Body mass index \> 35 kg/m2
Where this trial is running
Tanta, Elgharbia
- Tanta University Hospitals — Tanta, Elgharbia, Egypt (Recruiting)
Study contacts
- Study coordinator: Ahmed Ahmed Zahran, MBBCH
- Email: ahmad162088@med.tanta.edu.eg
- Phone: +20 101 997 6377
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.