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

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age45-95
SponsorSakarya University

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients undergoing hip farcture surgery

Disqualifiers

Chronic analgesics consumption

Patients contraindicated for neuraxial anesthesia

Alcohol and drug addiction

Allergies to local anesthetics and opioids

Trial design

Design model

Parallel

Treatments tested in this trial

  • PENG block with 0.25% bupivacaine guided by ultrasound.

    Procedure/Surgery

    PENG (Pericapsular nerve block) is a peripheral nerve block which is performed for patients with hip fractures aimed to prevent preoperative and postoperative pain. It is performed under sterile conditions under ultrasound guideance.

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: Group PENGExperimental treatment 1 intervention
Group B: Group ControlNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Preoperative Pain Scores and Opioid Consumption

Preoperative pain of patients will be assessed with NRS (Numeric Raitng Scale) which ranges from 0 (no pain) to 10 (the most severe pain imaginable).

Time frame
24 hours preoperatively

Secondary outcomes

1

Discharge Time

Time frame
From surgery to discharge up to 30 days
2

Postoperative Mortality and Morbidity

Postoperative complications such as infections, embolism, chronic pain and survival status

Time frame
30 days after surgery
3

Opioid Consumption

Opioid consumption will be assessed with patient controlled analgesia (PCA) device which measures analgesic drug consumption. Fentanyl consumption unit will be micrograms.

Time frame
24 hours preoperatively

Other outcomes

Sponsors and contacts

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