Skip to main content
Clinical Trials/NCT05136248
NCT05136248
Completed
Not Applicable

Comparison of Ultrasound Guided Intra-articular Steroid Injection and Pericapsular Nerve Group Block (PENG) in Patients With Chronic Hip Pain

Diskapi Teaching and Research Hospital1 site in 1 country60 target enrollmentApril 25, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hip Osteoarthritis
Sponsor
Diskapi Teaching and Research Hospital
Enrollment
60
Locations
1
Primary Endpoint
numerical rating scale (NRS) pain score
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The most common cause of hip joint dysfunction in the elderly is degenerative osteoarthritis of the hip. Innervation of the hip joint capsule is provided by the obturator nerve, the accessory obturator nerve, and the femoral nerve. With pericapsular nerve group block (PENG), by blocking the femoral nerve and the accessory obturator nerve, analgesia is successfully provided for the hip joint. Intra-articular injection of corticosteroids; It is used as an alternative to surgical interventions because it reduces inflammation and short-term pain and is a minimally invasive method. The investigators aim to compare and report patients who underwent ultrasound-guided intra-articular steroid injection and PENG block in terms of post-procedural pain scores and patient satisfaction.

Registry
clinicaltrials.gov
Start Date
April 25, 2020
End Date
December 20, 2021
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Selin Guven Kose

principal Investigator

Diskapi Teaching and Research Hospital

Eligibility Criteria

Inclusion Criteria

  • Hip pain NRS \> 4
  • No pathologies in the laboratory and coagulation parameters

Exclusion Criteria

  • Rheumatological disease with hip involvement
  • Systemic active infection
  • Malignancy
  • History of hip joint surgery
  • History of traumatic hip injury
  • Platelets values \< 150.000 / µl
  • History of bleeding disorder

Outcomes

Primary Outcomes

numerical rating scale (NRS) pain score

Time Frame: change from baseline to day 1, week 2, 4, 8 after the block

The 11-point NRS consists of numbers between 0 and 10 where 0 indicates "no pain" and 10 indicates "maximum pain." The patient is instructed to identify one number between 0 and 10, which is best representative of their pain intensity.

Secondary Outcomes

  • Quality of Life (WOMAC)(baseline to 8 weeks)

Study Sites (1)

Loading locations...

Similar Trials