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Suprainguinal Fascia Iliaca Block Versus PENG Block for Hip Arthroplasty Analgesia

U

University of Chile

Status

Completed

Conditions

Postoperative Pain
Postoperative Complications
Weakness, Muscle
Motor Activity

Treatments

Procedure: Ultrasound-guided pericapsular nerves group of the hip block
Procedure: Ultrasound-guided suprainguinal fascia iliaca nerve block

Study type

Interventional

Funder types

Other

Identifiers

NCT04402450
OAIC 1111/20

Details and patient eligibility

About

In recent years, suprainguinal fascia iliaca block (SFIB) has emerged as a reliable analgesic option for primary total hip arthroplasty (THA). In 2018, a new block was described, termed pericapsular nerve group block or PENG block, that selectively targets the articular branches of the femoral and obturator nerves while sparing their motor components. In this randomized trial, the investigators will compare US-guided SFIB and PENG block in patients undergoing primary THA. Since the main benefit of PENGB stems from its quadriceps-sparing effect, it was selected the incidence of quadriceps motor block (at 6 hours) as the primary outcome and the hypothesis that PENG block will result in significantly less motor block compared to SFIB.

Enrollment

40 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age between 18 and 80 years
  • American Society of Anesthesiologists classification 1-3
  • Body mass index between 20 and 35 (kg/m2)

Exclusion criteria

  • Adults who are unable to give their own consent
  • Pre-existing neuropathy (assessed by history and physical examination)
  • Coagulopathy (assessed by history and physical examination and, if deemed clinically necessary, by blood work up i.e. platelets ≤a100, International Normalized Ratio ≥01.4 or prothrombin time ≥ 50)
  • Renal failure (assessed by history and physical examination and, if deemed clinically necessary, by blood work up i.e. creatinine ≥ 100)
  • Hepatic failure (assessed by history and physical examination and, if deemed clinically necessary, by blood work up i.e. transaminases ≥ 100)
  • Allergy to local anesthetics (LAs)
  • Pregnancy
  • Prior surgery in the corresponding side of the inguinal or suprainguinal area
  • Chronic pain syndromes requiring opioid intake at home

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

40 participants in 2 patient groups

suprainguinal fascia iliaca block
Active Comparator group
Description:
Forty mL of levobupivacaine 0.25% with epinephrine 5 ug/mL will be injected cranial to the inguinal ligament between the fascia iliaca and the iliopsoas muscle.
Treatment:
Procedure: Ultrasound-guided suprainguinal fascia iliaca nerve block
Pericapsular nerve group block
Experimental group
Description:
Twenty mL of levobupivacaine 0.5% with epinephrine 5 ug/mL will be deposited in the anterior aspect of the iliac bone between its periosteum and the tendon of the iliopsoas muscle.
Treatment:
Procedure: Ultrasound-guided pericapsular nerves group of the hip block

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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