The aim of the study is to compare the analgesic effect of fascia iliaca compartment block (FIC) block and pericapsular nerve group (PENG) block in hip fracture pain control. The participants, caregivers, and assessors will be blinded to the type of block the participants receive. Patients aged 20 years or older with hip fracture scheduled for surgical treatment will be assessed for eligibility to participate the study. One hundred eligible patients will be included in the study after informed consents are obtained, and then randomly allocated into either FIC block or PENG block, with 50 patients in each group. Both blocks will performed under ultrasound guidance. The followings will be assessed: the numerical rating pain scale (NRS 0-10, 0: no pain, 10: worst pain imaginable) at before and after nerve block at different time points during rest and passive internal rotation of the fractured lower limb to neutral position from its typical external rotation deformity 30 mins after block (primary outcome). The degree of patient's satisfaction regarding nerve blocks and anesthesiologist's satisfaction regarding patient position during spinal anesthesia will also be assessed. The pain and use of rescue analgesics in the first 24 hours after operation will be recorded.
The aim of this study is to compare the analgesic effect of fascia iliaca compartment block (FIC) block and pericapsular nerve group (PENG) block in hip fracture pain control before operation. Methods This will be a randomized, assessor and participant-blinded study. After the patients give his /her informed consents, his/her baseline demographic data (gender, age, height, and body weight) and types of hip fracture will be recorded. Participants will be randomly allocated into either FIC block or PENG block by using the website RESEARCH RANDOMIZER (https://www.randomizer.org). One of the two anesthesiologists experienced in performed the FIC and PENG blocks will perform the nerve blocks. Only the anesthesiologist performing the nerve block and his assistant will be aware of which nerve block the participant receives immediately before performing nerve block by opening a sealed envelope. The assessors, in-charge anesthesiologists and nurse anesthetists, operation room personnel, surgeons and study participants will be all blinded to the randomization. On arrival of the operating theater, all participants will be sent to the nerve block area, where continuous electrocardiogram, pulse oximetry, and non-invasive intermittent blood pressure monitoring will be applied and an intravenous line will be established. Before any intervention, pain at rest and during the fractured lower limb being passively internal rotated in extension to neutral position from its usual externally rotated deformity by assessors will assessed using NRS. If the participant cannot tolerate passive internal rotation of his/her fractured limb due to pain, impossibility to perform the test will be recorded as well as the worst NRS score during these attempts. The same assessment will be performed every 10 mins for until 30 mins after completion of the nerve block. Then the patient will be sent to the operation room, where spinal anesthesia will be performed for the surgery.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
100
A linear ultrasound transducer is placed in a sagittal plane to identify the anterior superior iliac spine. By sliding the transducer medially, the fascia iliaca and abdominal internal oblique, sartorius, and iliopsoas muscles are identified. After identifying the "bow-tie sign", a 23-gauge needle (7mm, Nipro, Japan) is inserted in plane from caudal to cephalad until the needle tip penetrate the fascia iliaca. After negative aspiration, 0.35% ropivacaine 30mL with 1:400,000 epinephrine will be injected to separate the fascia iliaca and the iliacus muscle.
A curvilinear ultrasound transducer is initially place on the anterior inferior iliac spine and then aligned to the iliopubic eminence by rotating around 45 degree. In this view, the iliopubic eminence, iliapsoas muscle and tendon, pectineus muscle, femoral artery and vein will be identified. A 23-gauge needle (7mm, Nipro, Japan) is inserted in plane from lateral to medial until the needle tip in the musculofascial plane between the psoas tendon anteriorly and the pubic ramus posteriorly. After negative aspiration, 0.35% ropivacaine 20mL with 1:400,000 epinephrine will be injected.
Mackay Memorial Hospital
New Taipei City, Taiwan
Pain measurement at rest
Numerical pain rating scale (0-10, 0: no pain, 10: worst pain imaginable) at rest
Time frame: 30 minutes after nerve blocks
Pain measurement during internal rotation
Numerical pain rating scale (0-10, 0: no pain, 10: worst pain imaginable) during the fractured limb being passively internally rotated to neutral position from usual externally rotated deformity
Time frame: 30 minutes after nerve blocks
Pain measurement at rest
Numerical pain rating scale (0-10, 0: no pain, 10: worst pain imaginable) at rest
Time frame: 10 minutes after nerve block
Pain measurement during internal rotation
Numerical pain rating scale (0-10, 0: no pain, 10: worst pain imaginable) during the fractured limb being passively internally rotated to neutral position from usual externally rotated deformity
Time frame: 10 minutes after nerve block
Pain measurement at rest
Numerical pain rating scale (0-10, 0: no pain, 10: worst pain imaginable) at rest
Time frame: 20 minutes after nerve block
Pain measurement during internal rotation
Numerical pain rating scale (0-10, 0: no pain, 10: worst pain imaginable) during the fractured limb being passively internally rotated to neutral position from usual externally rotated deformity
Time frame: 20 minutes after nerve block
pain measurement during positioning for spinal anesthesia
Numerical pain rating scale (0-10, 0: no pain, 10: worst pain imaginable) during changing position from supine to lateral decubitus with flexion of the healthy hip
Time frame: Just before operation
pain measurement after operation
Numerical pain rating scale (0-10, 0: no pain, 10: worst pain imaginable)
Time frame: 6, 12, and 24 hours after operation
the time spending for performing spinal anesthesia
defined as starting of positioning maneuver to removal of spinal needle
Time frame: Just before operation
quality of position for spinal anesthesia
characterized as unsatisfied, satisfied, good, and excellent by the anesthesiologists performing the spinal anesthesia
Time frame: Just before operation
the first time of pain perceived by the patient after operation
the time interval between the end of operation and pain first perceived by the patient
Time frame: Within 48 hours after operation
the time of first request for rescue analgesics after operation
the time interval between the end of operation and the first request for rescue analgesics
Time frame: Within 48 hours after operation
total consumption of rescue analgesics within 24 hours after the operation
total consumption of rescue analgesics within 24 hours after the operation
Time frame: Within 24 hours after the operation
the first time of ambulation after operation
the time interval between the end of operation and the first time the patient can ambulate with assistance after operation
Time frame: Within 72 hours after operation
the time spending for nerve block
defined as from contact of skin by the ultrasound transducer to removal of the needle
Time frame: Before operation
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