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Dexamethasone for ESPB in Total Hip Arthroplasty

P

Poznan University of Medical Sciences (PUMS)

Status and phase

Completed
Phase 4

Conditions

Hip Arthropathy
Hip Osteoarthritis
Hip Arthritis

Treatments

Drug: Dexamethasone 4mg
Drug: 0.9%NaCl

Study type

Interventional

Funder types

Other

Identifiers

NCT06789042
10/2024

Details and patient eligibility

About

Effect of adding Dexamethasone to Erector Spinae Plane Block in Patients undergoing Total Hip Arthroplasty

Full description

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

Enrollment

60 patients

Sex

All

Ages

18 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients scheduled for total hip arthroplasty
  • patients aged >65 and <100 years
  • patients able to provide informed consent
  • patients able to reliably report symptoms to the research team

Exclusion criteria

  • inability to provide first-party consent due to cognitive impairment or a language barrier

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

60 participants in 2 patient groups

Control group
Active Comparator group
Description:
Ultrasound-guided ESPB - 20ml 0,2% ropivacaine + 2ml 0.9% NaCl
Treatment:
Drug: 0.9%NaCl
Dexamethasone
Active Comparator group
Description:
Ultrasound-guided ESPB - 20ml 0,2% ropivacaine + 4mg Dexamethasone
Treatment:
Drug: Dexamethasone 4mg

Trial contacts and locations

1

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Central trial contact

Malgorzata Reysner, MD PhD

Data sourced from clinicaltrials.gov

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