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Erector Spinae vs. PENG Block for Total Hip Arthroplasty

P

Poznan University of Medical Sciences (PUMS)

Status and phase

Completed
Phase 4

Conditions

Hip Arthropathy
Hip Osteoarthritis
Hip Pain Chronic

Treatments

Drug: Ropivacaine 0.2% Injectable Solution Erector Spinae Plane Block
Drug: Control Test
Drug: Ropivacaine 0.2% Injectable Solution - PENG block

Study type

Interventional

Funder types

Other

Identifiers

NCT06083428
11/2023

Details and patient eligibility

About

Effect of PENG block and ESPB on pain management, and NLR and PLR following knee arthroplasty

Full description

Hip arthroplasty is one of the most common orthopedic procedures, especially in elderly patients, due to the deformation of joints. Patients may complain of severe pain due to surgical trauma and prosthesis. Regional anesthesia methods may be performed to reduce the inflammatory response, opioid consumption, and opioid-related side effects.

In recent years, the influence of regional anesthesiology on reducing the inflammatory response after surgical procedures has been emphasized. However, very few studies have evaluated the effect of various methods of anesthesia on the NLR.

This is the first study to investigate the effect of regional anesthesia on the NLR and PLR in patients undergoing hip replacement surgery.

Enrollment

90 patients

Sex

All

Ages

20 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with ASA classification I-III, Aged 20-90 years, Who will be scheduled for hip arthroplasty under spinal anesthesia.

Exclusion criteria

  • Patients who have a history of bleeding diathesis, Take anticoagulant therapy, have a History of chronic pain before surgery, have Multiple trauma, cannot assess their pain (dementia), have been operated on under general anesthesia, have an infection in the area and do not accept the procedure

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

90 participants in 3 patient groups

PENG Block group
Active Comparator group
Description:
ultrasound guided PENG block - 20ml 0,2% ropivacaine
Treatment:
Drug: Ropivacaine 0.2% Injectable Solution - PENG block
ESPB group
Active Comparator group
Description:
ultrasound guided erector spinae plane block - 20ml 0,2% ropivacaine
Treatment:
Drug: Ropivacaine 0.2% Injectable Solution Erector Spinae Plane Block
Control group
Active Comparator group
Description:
Only spinal anesthesia - No peripheral nerve block
Treatment:
Drug: Control Test

Trial contacts and locations

1

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Central trial contact

Malgorzata Domagalska, Ph.D.

Data sourced from clinicaltrials.gov

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