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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05136248
Other study ID # 84/18
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 25, 2020
Est. completion date December 20, 2021

Study information

Verified date April 2023
Source Diskapi Teaching and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date December 20, 2021
Est. primary completion date August 20, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
intraarticular injection
Ultrasound-guided intraarticular injection
peng block
Ultrasound-guided PENG block

Locations

Country Name City State
Turkey Diskapi Yildirim Beyazit Training and Research Hospital Ankara

Sponsors (1)

Lead Sponsor Collaborator
Diskapi Teaching and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Other Change in Harris Hip Score (HHS) The Harris Hip Score (HHS) is a joint-specific measure, and it consists of two sections: questions and a physical examination, including a range of motion and deformity items. The score has a maximum of 100 points with a maximum of 44 points for pain, 47 for function, 4 points for absence of deformity, and 5 points for a range of motion. The highest score of 100 points indicates the best function and no pain. baseline to 8 weeks
Primary numerical rating scale (NRS) pain score 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. change from baseline to day 1, week 2, 4, 8 after the block
Secondary Quality of Life (WOMAC) The Western Ontario and McMaster Universities (WOMAC) is a self-administered health status measure and consists of 24 items divided into three domains, which are pain, stiffness, and physical function, validated to patients with hip or knee osteoarthritis baseline to 8 weeks
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