Comparing two methods for pain relief during hip fracture surgery
Ultrasound Guided Fascia Iliaca Block Versus Intravenous Dexmedetomidine and Ketamine for Positioning Fracture Femur Patients During Spinal Anesthesia: Randomized Comparison Study
NA · Minia University · NCT05705726
This study is testing two different pain relief methods to see which one works better for people aged 18-60 with hip fractures during surgery.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 70 (estimated) |
| Ages | 18 Years to 60 Years |
| Sex | All |
| Sponsor | Minia University (other) |
| Locations | 1 site (Minya) |
| Trial ID | NCT05705726 on ClinicalTrials.gov |
What this trial studies
This study aims to compare the effectiveness of two analgesic techniques—fascia iliaca block and intravenous dexmedetomidine combined with ketamine—used to alleviate pain during the positioning of patients for spinal anesthesia in hip fracture surgeries. Proximal femur fractures are common in the elderly, and managing pain effectively is crucial for improving patient experience and outcomes. The study will involve patients aged 18-60 with hip fractures, assessing the analgesic effects of the two methods prior to surgery. The goal is to determine which method provides better pain relief during the critical positioning phase.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18-60 who have sustained a hip fracture.
Not a fit: Patients with cognitive impairments, allergies to local anesthetics, or those who have received analgesics within the last 12 hours 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 surgery for hip fractures.
How similar studies have performed: While there have been studies on various analgesic techniques, this specific comparison of fascia iliaca block versus intravenous dexmedetomidine and ketamine is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Aged 18-60 years. 2. Hip fractures 3. Both sexes. Exclusion Criteria: 1. Patient refusal 2. Allergy to local anesthetics 3. Bleeding diathesis or history of anticoagulant use. 4. impaired cognition or dementia 5. . Infection of the skin at the site of needle punctures area 6. multiple fractures 7. Any previous analgesic administration during the last 12 hours
Where this trial is running
Minya
- Minia University Hospital — Minya, Egypt (RECRUITING)
Study contacts
- Principal investigator: hassan m. hetta, lecturer — Minia University, faculty of medicine
- Study coordinator: hassan m. hetta, lecturer
- Email: hassan.hetta@mu.edu.eg
- Phone: 1010901114
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.