Comparıson Of The Effects Of Perıcapsulary Nerve Group Block (Peng Block) And Lumbar Erector Spına Plan Block (Lesp Block) On Postoperatıve Opıoıd Consumptıon

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age65+
SponsorSakarya University

About this trial

The aim is to demonstrate that lumbar ESP block provides more effective postoperative analgesia than PENG block in geriatric patients with hip fractures, and reduces postoperative opioid consumption more than PENG block

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

patients with hip fractures

over 65 years old

Disqualifiers

long-term surgery

Patients who do not want regional anesthesia

bleeding disorder disease

wound in the operation area

Trial design

Design model

Parallel

Treatments tested in this trial

  • Postoperative pain assessment of patients who underwent block

    Procedure/Surgery

    Postoperative pain assessment of patients who underwent block

Treatment groups

70 Participants
are divided into 2 treatment groups
Group A: pericapsular nerve group block (peng block)Experimental treatment 1 intervention
Group B: lumbar erector spinae plane block(lesp block)Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

postoperative pain

To evaluate postoperative pain after two different block applications in patients undergoing hip fracture surgery.Evaluation of patients' postoperative 30th minute, 2nd hour, 6th hour, 12th hour and 24th hour verbal analog scores.To examine the total fentanyl consumption, acetaminophen consumption, and nonsteroidal anti-inflammatory drug consumption of patients in the postoperative 24 hours.

Time frame
6 month

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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