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Genicular Nerve Block in Juvenile Idiopathic Arthritis

Genicular Nerve Block in Juvenile Idiopathic Arthritis

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04687930
Enrollment
104
Registered
2020-12-29
Start date
2020-12-01
Completion date
2021-02-15
Last updated
2021-07-23

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

Conditions

Juvenile Idiopathic Arthritis, Persistent Knee Arthritis, no Intra-articular Injection in the Last 3 Months, no Other Cause for Chronic Kneearthritis

Keywords

Juvenile rheumatoid arthritis, knee joint, Nerve block

Brief summary

N=104 juvenile idiopathic arthritis patients diagnosed after ILAR criteria with unilateral persistent knee arthritis. They will be randomly assigned into two groups; group 1 will receive genicular nerve block, group 2 intra-articular triamcinolone. Both groups will be examined by SOLAR ultrasound scoring system, Visual analogue scale and Lysholm score at 0, 2 and 12 weeks. A semi-quantitative score will be used to assess tenderness and swelling at the same intervals.

Interventions

nerve block of the genicular nerve at 3 points around the inflamed knee using ultrasound.

Triamcinilone injection into the knee joint under ultrasound guidance.

Sponsors

Sohag University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
No minimum to 16 Years
Healthy volunteers
No

Inclusion criteria

* juvenile idiopathic arthritis with persistent knee arthritis * age below 16

Exclusion criteria

* severe knee osteoarthritis * peripheral neuropathy, * psoriatic arthritis, * those under anticoagulant therapy, skin infection, * prior knee injection in the last 3 months3 * those who have an allergy to Bupivacaine

Design outcomes

Primary

MeasureTime frameDescription
Change in SOLAR score over timeBaseline, 2 weeks and 12 weeksscore to assess ultrasound parameters of the knee including power doppler and grey scale measures
Change in visual analogue scale over timeBaseline, 2 weeks and 12 weeksa graded score for pain evaluation filled by the patient graded from 0 to 10
Change in Lysholm score over timeBaseline, 2 weeks and 12 weeksa score to assess knee function. This questionnaire has 8 domains. A score between 95 and 100 means excellent functional performance, good 84-94, fair 65-83 and poor \<64
Change in semiquantitative score for swelling and tenderness over timeBaseline, 2 weeks and 12 weeksA score graded from 0 to 3; score 0 means no swelling nor tenderness and 3 means maximum swelling and tenderness

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026