Actively Recruiting

Phase Not Applicable
Age: 60Years +
All Genders
NCT05660603

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

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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

Age: 60Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Shereen E Abd Ellatif

Zagazig, Alsharqia, Egypt, 4115

Actively Recruiting

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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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