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The Predictive Value of Ultrasonographic Quadriceps Muscle Parameters for Genicular Nerve Block Outcomes in Knee Osteoarthritis

The Role of Quadriceps Muscle Architecture Parameters in Predicting the Success of Genicular Nerve Block in Patients With Chronic Knee Osteoarthritis Pain

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07781059
Enrollment
41
Registered
2026-08-24
Start date
2025-06-01
Completion date
2026-04-01
Last updated
2026-08-24

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

Conditions

Knee Arthritis Osteoarthritis, Chronic Knee Pain

Keywords

knee osteoartritis, genicular nerve block, quadriceps muscle architecture, ultrasound -guided, pain management, WOMAC, EQ-5D, Numeric Rating Scale

Brief summary

The goal of this observational study is to learn whether thigh muscle structure can help predict pain relief after a genicular nerve block in people with knee osteoarthritis. A genicular nerve block is an injection used to reduce pain signals from the knee. The main questions are: * Are muscle thickness, fiber length, and fiber angle linked to pain relief after the procedure? * Are these muscle measurements linked to changes in physical function and quality of life? Participants are adults aged 50 to 80 with long-term pain from osteoarthritis in one knee. They are already scheduled to receive a genicular nerve block as part of their regular medical care. The study does not assign participants to receive this procedure. Before the procedure, researchers will use ultrasound to measure the vastus lateralis muscle in the thigh. Participants will also answer questions about pain, daily function, and quality of life. Researchers will repeat these assessments after 1 hour, 3 weeks, and 3 months. Pain relief will be considered successful when pain is at least half as severe as it was before the procedure.

Interventions

Ultrasound-guided genicular nerve block targeting the superomedial, superolateral, and inferomedial genicular nerves was performed as part of routine clinical management for chronic knee osteoarthritis.

Sponsors

Marmara University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Age between 50 and 80 years * Unilateral symptomatic knee osteoarthritis * Chronic knee pain for at least 3 months * Clinical and radiographic confirmation of knee osteoarthritis * Kellgren-Lawrence grade 3 or 4 knee osteoarthritis * Inadequate clinical response despite analgesic therapy and physical therapy * Clinical indication for genicular nerve block

Exclusion criteria

* History of surgery involving the knee region * Bilateral symptomatic knee osteoarthritis * Intra-articular knee injection within the previous 3 months * Systemic disease that could affect study assessments * Systemic or local infection * Coagulation disorder * Failure to provide written informed consent

Design outcomes

Primary

MeasureTime frameDescription
Change in Pain Intensity Assessed by the Numeric Rating Scale (NRS)Baseline , 3 weeks, and 3 monthsPain intensity will be assessed using an 11-point Numeric Rating Scale ranging from 0 (no pain) to 10 (worst imaginable pain). Changes from baseline will be evaluated following ultrasound-guided genicular nerve block. Lower scores indicate lower pain intensity.

Secondary

MeasureTime frameDescription
Baseline Vastus Lateralis Muscle ThicknessBaselineVastus lateralis muscle thickness assessed by ultrasound and recorded in millimeters (mm).
Baseline Vastus Lateralis Pennation AngleBaselineDescription: Vastus lateralis pennation angle assessed by ultrasound and recorded in degrees (°).
Baseline Vastus Lateralis Fascicle LengthBaselineDescription: Vastus lateralis fascicle length assessed by ultrasound and recorded in millimeters (mm).
Change in Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) ScoreBaseline, 3 weeks, and 3 months after the procedureDescription: Pain, stiffness, and physical function related to knee osteoarthritis will be assessed using the 24-item WOMAC questionnaire. The total score ranges from 0 to 96, with higher scores indicating greater pain, stiffness, and functional impairment. Changes from baseline will be evaluated following ultrasound-guided genicular nerve block.
Change in Health-Related Quality of Life Assessed by the EQ-5DBaseline, 3 weeks, and 3 months after the procedureDescription: Health-related quality of life will be assessed using the EQ-5D questionnaire. Responses will be converted into an EQ-5D index score, where higher scores indicate better health status. A score of 1 represents full health, 0 represents a health state equivalent to death, and negative scores represent health states considered worse than death. Changes from baseline will be evaluated following ultrasound-guided genicular nerve block.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 25, 2026