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US-guided FICB After Hip Fracture: the Effect of the Local Anesthetic Volume on the Quality of Preoperative Analgesia

U

University Tunis El Manar

Status

Completed

Conditions

Hip Fractures

Treatments

Procedure: supra inguinal fascia iliaca block

Study type

Interventional

Funder types

Other

Identifiers

NCT04692857
UTEM VOL FIBSI

Details and patient eligibility

About

participants were randomly divided into three groups : group 30 , group 40 and group 50 . for all the three groups an ultrasound guided supra-inguinal fascia iliaca block had been performed.

for group 30 ,a volume of 30 ml of 0,2 % ropivacaine had been injected for group 40 ,a volume of 40 ml of 0,2 % ropivacaine had been injected for group 50 ,a volume of 50 ml of 0,2 % ropivacaine had been injected

Full description

participants were randomly divided into three groups : group 30 , group 40 and group 50 . for all the three groups an ultrasound guided supra-inguinal fascia iliaca block had been performed.

A linear ultrasound probe was placed in the sagittal plane to obtain an image of the superior iliac spine.the fascia iliaca and sartorious,iliopsoas,and oblique internal muscles were identified by sliding the probe medially. After identifiying the "bow-tie sign"formed by the muscle fascias , an 50 mm needle was introduced 1-2 cm inferior to the inguinal ligament.using an in-plane approch, the fascia iliaca was penetrated and hydrodissected , separating the fascia iliaca from the iliac muscle. in this created space a total volume of 30 ml, 40ml or 50ml of 0.2% ropivacaine was injected , respectively to group 30 ,group 40 and group 50 .

pain score at rest and with a straight leg raise of the affected limb to 15 degrees were assessed before and 30 minutes after block performance.

Enrollment

75 patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients aged above 65 years , american society of anesthesiologists physical status I to III , and with body mass index (BMI) of 35 kg/m² or less , undergoing hip fracture surgical repair .

Exclusion criteria

  • inability or refusal to sign informed consent
  • younger than 65 years
  • BMI greater than 35 kg/m²
  • presence of contraindications for regional nerve block or spinal anesthesia
  • impaired cognition or dementia
  • multiple fractures

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

75 participants in 3 patient groups

group 30
Experimental group
Description:
participants received a supra inguinal fascia iliaca compartment block with 30 ml of 0.2% ropivacaine
Treatment:
Procedure: supra inguinal fascia iliaca block
group 40
Experimental group
Description:
participants received a supra inguinal fascia iliaca compartment block with 40 ml of 0.2% ropivacaine
Treatment:
Procedure: supra inguinal fascia iliaca block
group 50
Experimental group
Description:
participants received a supra inguinal fascia iliaca compartment block with 50 ml of 0.2% ropivacaine
Treatment:
Procedure: supra inguinal fascia iliaca block

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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