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

S

Sakarya University

Status

Not yet enrolling

Conditions

over65years
Lumbar Erector Spinae Plane Block
Hipfracture
Pengblock

Treatments

Procedure: Postoperative pain assessment of patients who underwent block

Study type

Interventional

Funder types

Other

Identifiers

NCT06995079
PENGVSLESP

Details and patient eligibility

About

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

Enrollment

70 estimated patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients with hip fractures
  • over 65 years old

Exclusion criteria

  • long-term surgery
  • Patients who do not want regional anesthesia
  • bleeding disorder disease
  • wound in the operation area

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

70 participants in 2 patient groups

pericapsular nerve group block (peng block)
Experimental group
Description:
The patient will first be taken to the block room in the operating room.In this group, patients will be given a Peng block before surgery.The patient will then be taken to the operating room and spinal anesthesia will be applied.Postoperative analgesia requirement will be assessed
Treatment:
Procedure: Postoperative pain assessment of patients who underwent block
lumbar erector spinae plane block(lesp block)
Experimental group
Description:
The patient will first be taken to the block room in the operating room.In this group, patients will be given a lumbar erector spinae plane block before surgery.The patient will then be taken to the operating room and spinal anesthesia will be applied.Postoperative analgesia requirement will be assessed
Treatment:
Procedure: Postoperative pain assessment of patients who underwent block

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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