Actively Recruiting
Circum-Psoas Blocks Versus Combined Lumbar and Sacral Plexus Blocks in Hip Fracture Surgery
Led by Zagazig University · Updated on 2025-07-17
63
Participants Needed
1
Research Sites
171 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Hip fracture (HF) is one of the major worldwide problems that constitute a significant mortality rate, ranging from 14- 36% in the first year after injury, and is associated with profound temporary and sometimes permanent impairment of independence and quality of life in the geriatric population. Surgical treatment is considered the best option for patients with hip fractures,s especially in the elderly, however, it is associated with moderate to severe postoperative pain. Pain is one of the main factors limiting ambulation, increasing the risk of thromboembolism by immobility and causing metabolic changes that affect other systems. Therefore, individualized pain management with the use of appropriate analgesic techniques is of paramount importance. Moreover, early intervention of rehabilitation aiming at a better postoperative recovery may reduce the length of hospital stay and return to daily. Effective pain management is one of the crucial components in enhanced recovery after surgery (ERAS). • Numerous regional anesthetic techniques have been used to provide analgesia following hip fracture surgery, including intrathecal morphine, epidural analgesia, fascia iliaca block, lumber plexus block, and sacral plexus block, however, each of these techniques has specific limitations that prevent them from being the analgesic technique of choice for hip fracture surgery. To our knowledge, there is no study done to compare circum-psoas block versus the combined lumbar and sacral plexus blocks as pre-emptive analgesia in patients undergoing hip fracture surgery under general anesthesia.
CONDITIONS
Official Title
Circum-Psoas Blocks Versus Combined Lumbar and Sacral Plexus Blocks in Hip Fracture Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient acceptance
- Body mass index (BMI) of 30 kg/m2 or less
- American Society of Anesthesiologists (ASA) physical status I to III
- First unilateral surgery for hip fracture including femoral neck, intertrochanteric, or subtrochanteric fracture
- Planned hip fracture surgery within 24 to 72 hours under general anesthesia
You will not qualify if you...
- Multiple trauma, multiple fractures, or pathological fractures
- Prosthetic fracture or use of bone-cement fixation during surgery
- Scheduled for bilateral hip fracture surgery
- Pre-existing neurological deficit in the lower extremity
- Contraindications for peripheral nerve block (infection at needle site, bleeding disorders, allergy to local anesthetics)
- History of chronic pain and use of analgesics
- History of cognitive dysfunction or mental illness
AI-Screening
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Trial Site Locations
Total: 1 location
1
Shereen E Abd Ellatif
Zagazig, Alsharqia, Egypt, 4115
Actively Recruiting
Research Team
S
Shereen E Abd Ellatif, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
3
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