Ultrasound-Guided Nerve Block for Hip Fracture Pain
Analgesic Efficacy of Ultrasound-Guided Deep Iliacus Plane Block in Patients Undergoing Hip Fracture Surgery
Recruiting
N/AInterventional Study
Pain Management
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
52 (estimated)
Sponsor
Kanuni Sultan Suleyman Training and Research Hospital · Other
Who this trial is looking for
This trial is looking for adults scheduled for hip fracture surgery. Participants will receive either a nerve block for pain relief or a placebo treatment after their surgery.
Are You a Good Fit for This Trial?
You may be able to join if
I am 18 years or older
I am scheduled for hip fracture surgery
I can understand and use the pain rating scale
I can provide consent or have a representative who can
You may not be able to join if
I have a serious health issue (ASA IV or higher)
I need emergency surgery
I have a bleeding disorder or take blood thinners
I have an infection where the needle will go
I am allergic to local anesthetics
I have nerve or muscle problems in my leg
I cannot understand the pain rating scale
I refuse to participate
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
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Hip fracture surgery is commonly associated with moderate to severe postoperative pain, which may delay mobilization and increase the need for opioid analgesics. The deep iliacus plane block is a recently described ultrasound-guided regional anesthesia technique designed to provide analgesia by allowing local anesthetic spread toward the femoral nerve, lateral femoral cutaneous nerve, and articula…
Hip fracture surgery is commonly associated with moderate to severe postoperative pain, which may delay mobilization and increase the need for opioid analgesics. The deep iliacus plane block is a recently described ultrasound-guided regional anesthesia technique designed to provide analgesia by allowing local anesthetic spread toward the femoral nerve, lateral femoral cutaneous nerve, and articular branches supplying the hip.
This prospective, randomized, double-blind, sham-controlled clinical trial will evaluate the analgesic efficacy of the deep iliacus plane block in adult patients undergoing hip fracture surgery under spinal anesthesia. After surgery, participants will be randomly assigned to receive either an ultrasound-guided deep iliacus plane block with local anesthetic or a sham block with normal saline.
All participants will receive standardized multimodal postoperative analgesia, including patient-controlled analgesia. The primary objective is to determine whether the deep iliacus plane block reduces postoperative opioid consumption during the first 24 hours after surgery. Postoperative pain scores, rescue analgesic requirements, sensory distribution, motor block, nausea and vomiting, quality of recovery, patient satisfaction, and block-related complications will also be evaluated.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Age 18 years or older
* Scheduled to undergo unilateral hip fracture surgery under spinal anesthesia
* American Society of Anesthesiologists (ASA) physical status I-III
* Ability to understand and use the Numerical Rating Scale and patient-controlled analgesia device
* No cont…
Inclusion Criteria:
* Age 18 years or older
* Scheduled to undergo unilateral hip fracture surgery under spinal anesthesia
* American Society of Anesthesiologists (ASA) physical status I-III
* Ability to understand and use the Numerical Rating Scale and patient-controlled analgesia device
* No contraindication to spinal anesthesia or the deep iliacus plane block
* Written informed consent provided by the participant or legally authorized representative
Exclusion Criteria:
* ASA physical status IV or higher
* Emergency surgery
* Coagulopathy, bleeding diathesis, or anticoagulant treatment that contraindicates spinal anesthesia or peripheral nerve block
* Infection at the planned needle insertion site
* Known allergy to local anesthetics or any study medication
* Pre-existing peripheral neuropathy, neurological disorder, or motor deficit involving the operated lower extremity
* Inability to understand or use the Numerical Rating Scale or patient-controlled analgesia device
* Cognitive impairment or communication difficulty preventing reliable postoperative assessment
* Refusal to participate
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