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PENG Block Plus Lateral Femoral Cutaneous Nerve Block for Posterolateral-approached Total Hip Arthroplasty

Not Applicable
Completed
Conditions
Pain
Acute Pain
Analgesia
Postoperative Complications
Postoperative Pain
Hip Arthropathy
Registration Number
NCT05432011
Lead Sponsor
Campus Bio-Medico University
Brief Summary

This study aims to analyze the effect of Pericapsular Nerve Group (PENG) Block combined with lateral femoral cutaneous nerve block vs. PENG block combined with wound infiltration for analgesia after elective hip replacement performed with a posters-lateral approach.

Half of participants will receive a PENG Block combined with femoral lateral cutaneous nerve block, while the other half will receive PENG Block combined with wound infiltration

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
50
Inclusion Criteria
  • Elective hip replacement surgery performed with a poster-lateral approach
  • ASA physical status score < 4
Exclusion Criteria
  • Contraindications to regional anesthesia
  • ASA physical status score ≥ 4
  • Patient's refusal or inability to sign the informed consent
  • Allergies to any drug provided by the study protocol

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Static Pain Score24 hours

A numerical rating scale (NRS) from 0 (no pain) to 10 (worst imaginable pain) will be used to evaluate pain at rest during 24 hours after surgery

Dynamic Pain Score24 hours

A numerical rating scale (NRS) from 0 (no pain) to 10 (worst imaginable pain) will be used to evaluate pain on movement during 24 hours after surgery

Secondary Outcome Measures
NameTimeMethod
Range of hip motion24 hours

Degrees of hip flexion

Morphine consumption6 days

Total of intravenous morphine (expressed in milligrams) administered during the entire hospitalization

Ability to start physiotherapy during the first postoperative day24 hours

YES: the patient was able to start physiotherapy NO: the patient was not able to start physiotherapy during the first postoperative day due to pain or motor block

Quadriceps Strength24 hours

Ability to flex the knee against gravity

Ability to ambulate with the help of a walker during the first postoperative day24 hours

YES: The patient was able to ambulate with the help of a walker NO: The patient was not able to ambulate with the help of a walker due to pain or motor block

Incidence of block complications24 hours

Any complications or side effects of the blocks, such as local infection, intravascular injection of local anesthetics and immediate systemic toxicity.

Moreover, incidence of nausea, vomiting and postoperative respiratory depression will be recorded

Hospital Length of Stay6 days

Total Hospital length of Stay (expressed in days)

Trial Locations

Locations (1)

Campus Bio-medico University Hospital Foundation

🇮🇹

Rome, Italy

Campus Bio-medico University Hospital Foundation
🇮🇹Rome, Italy

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