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Comparison of the Efficacy of Phenol Block and Corticosteroid-Local Anesthetic Block Applied to the Genicular Nerve

Comparison of the Efficacy of Ultrasound-Guided Phenol Block and Corticosteroid-Local Anesthetic Block Applied to the Genicular Nerve in Patients With Knee Osteoarthritis

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06265675
Enrollment
88
Registered
2024-02-20
Start date
2024-01-24
Completion date
2025-06-24
Last updated
2024-02-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Knee Osteoarthritis

Keywords

Genicular nerve, Phenol, Knee Osteoarthritis, Neurolysis, Nerve Blockage

Brief summary

There are different neurolysis methods. Aim of this study is to compare two different methods, phenol block and corticosteroid local anesthetic block.

Detailed description

Knee osteoarthritis is one of most frequent reason of knee pain. There are different treatment methods such as analgesic drug treatment, physical therapy techniques, intraarticular injections and neurolysis techniques. In this study, we will compare neurolysis techniques these are phenol block and corticosteroid local anesthetic block.

Interventions

DRUGPhenol

Chemical neurolysis

Chemical neurolysis with corticosteroid

DRUGLidocain

Chemical neurolysis with local anesthetic

Sponsors

Gaziler Physical Medicine and Rehabilitation Education and Research Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
50 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients with knee osteoarthritis must have pain at least 6 months * NRS score of knee pain equal or more than 5 * At least grade 3 in Kellgren-Lawrence grading scale * Non responsive to life style change, weight control, exercises program, medical treatment and the other conservative treatments (physical therapy, intraarticular injections) * Decreasing at NRS score more than %50 after diagnostic block * Those who accept the consent form

Exclusion criteria

* Patients who have acute knee injury * Surgery history in knee * Connective tissue disease that affect knee * Sciatica * Injection story in last 3 months * Psychiatric or neurologic diseases that affect study * Septic arthritis, active local or systemic infection * Coagulopathy * Pregnancy * Allergic reaction

Design outcomes

Primary

MeasureTime frameDescription
Numeric Rating Scale (NRS)Before the intervention, 4 weeks after the intervention and 3 months laterAverage knee pain is assessed using an 11-point NRS with terminal descriptors of no pain (score 0) and extreme pain (score 10).

Secondary

MeasureTime frameDescription
Western Ontario and McMaster Universities Arthritis Index (WOMAC)Before the intervention, 4 weeks after the intervention and 3 months laterWe will use the WOMAC in the Likert version where question are scored on a scale of 0-4, which correspond to: None (0), Mild (1), Moderate (2), Severe (3), and Extreme (4). The scores for each subscale are summed up, with a possible score range of 0-20 for Pain, 0-8 for Stiffness, and 0-68 for Physical Function. So the sum of the scores ranges from 0 (the best) to 96 (the worse).
Patient Global Impression of Change (PGIC)4 weeks after the intervention and 3 months laterThe PGIC in pain and function will be measured with a 5-point Likert scale (1-5) on the applicable follow up visits. The patients will be asked to rate the following statements: Please imagine how you would have described your pain intensity before the procedure. How do you feel today as compared to baseline (Start of the study) as far as your knee pain caused by OA is concerned? Please imagine how you would have described the functionality of your knee before the procedure. How do you feel today as compared to baseline (start of the study) as far as your knee functionality caused by OA is concerned? The options on the Likert scale are: much better slightly better no change slightly worse much worse
Sixt Minute Walk Test (6MWT)Before the intervention, 4 weeks after the intervention and 3 months laterA 6 minute walk test is a submaximal exercise test that measures the distance walked over the span of 6 minutes.
The Timed-Up and Go testBefore the intervention, 4 weeks after the intervention and 3 months laterThis test measures the dynamic balance and functional mobility in older adults.A patient getting up from a chair from the sitting to the bipedal position, walking three meters, turning, returning, and sitting on the chair again.
Frequency of analgesic usageBefore the intervention, 4 weeks after the intervention and 3 months laterAssessment of analgesic number that used by patient with knee osteoarthritis

Countries

Turkey (Türkiye)

Contacts

Primary ContactRabia Layık
rabialyk@gmail.com+905314087679

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026