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Preoperative Analgesia: The Effectiveness of the PENG Block in Patients With Hip Fractures

S

Sakarya University

Status

Not yet enrolling

Conditions

Hip Fracture Surgeries

Treatments

Procedure: PENG block with 0.25% bupivacaine guided by ultrasound.

Study type

Interventional

Funder types

Other

Identifiers

NCT07003633
E-43012747-050.04-463726-205

Details and patient eligibility

About

The aim is to provide effective preoperative analgesia in patients undergoing surgical procedures due to hip fractures by administering a pericapsular nerve group (PENG) block under ultrasound guidance. This approach seeks to increase patient satisfaction, reduce analgesic requirements, enable earlier discharge, and decrease morbidity and mortality.

Enrollment

60 estimated patients

Sex

All

Ages

45 to 95 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients undergoing hip farcture surgery

Exclusion criteria

  • Chronic analgesics consumption
  • Patients contraindicated for neuraxial anesthesia
  • Alcohol and drug addiction
  • Allergies to local anesthetics and opioids
  • Patients who refuses to participate in the study

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

Group PENG
Experimental group
Description:
Group PENG will involve the patients who will be performed PENG block 24 hours before surgery.
Treatment:
Procedure: PENG block with 0.25% bupivacaine guided by ultrasound.
Group Control
No Intervention group
Description:
Group Control will involve the patients who will not be performed PENG block preoperatively.

Trial contacts and locations

1

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Central trial contact

Alim Miniksar, M.D.

Data sourced from clinicaltrials.gov

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