PENG Block Combined to Wound Infiltration for Hip Replacement

Campus Bio-Medico University of Rome

Status: Completed

Conditions: Postoperative Complications; Postoperative Pain; Hip Arthropathy; Analgesia; Acute Pain; Pain

Treatments: Procedure: PENG block; Procedure: Wound Infiltration

Study type: Interventional

Funder types: Other

Identifiers

NCT04306133

29/20 PAR ComEt CBM

Details and patient eligibility

About

This study analyze the effect of Pericapsular Nerve Group (PENG) Block combined to wound infiltration for analgesia after elective hip replacement.

Half of participants will receive a PENG Block combined with wound infiltration, while the other half will receive wound infiltration alone.

Enrollment: 60 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Elective hip replacement surgery
• ASA physical status score < 4

Exclusion criteria

• Contraindications to regional anesthesia
• ASA physical status score ≥ 4
• Patient's refusal or inability to sing the informed consent
• Pre-operatively therapy with opioids
• Allergies to any drug provided by the study protocol

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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60 participants in 2 patient groups

PENG BLOCK AND WOUND INFILTRATION

Experimental group

Description:

Participants receiving PENG block combined to wound infiltration

Treatment:

Procedure: PENG block

Procedure: Wound Infiltration

WOUND INFILTRATION

Active Comparator group

Description:

Participants receiving wound infiltration alone

Treatment:

Procedure: Wound Infiltration