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Genicular Nerve Block in Rheuamtoid Arthritis

Registration Number
NCT04361513
Lead Sponsor
Sohag University
Brief Summary

N=64 RA patients either early or established disease diagnosed after ACR/EULAR criteria 2010 with unilateral persistent knee arthritis. They were randomly assigned into two groups; group 1 received genicular nerve block, group 2 intra-articular triamcinolone. Both groups were examined by SOLAR scoring system, Visual analogue scale (VAS) and Lysholm score at 0, 2 and 12 weeks. A semi-quantitative score was used to assess tenderness and swelling at the same intervals.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
64
Inclusion Criteria
  • RA patients
  • Age > 18
  • unilateral persistent knee arthritis
Exclusion Criteria
  • Participants with severe knee osteoarthritis
  • peripheral neuropathy
  • psoriatic arthritis
  • skin infection
  • or those who have allergy for Bupivacaine

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Nerve block grouptriamcinolone 40 milligrams (Kenacort, Bristol Myers Squip)3 point genicular nerve block under ultrasound guidance. half ml of Bupivacaine hydrochloride 0.5% (Marcaine, Pfizer) was injected in each point.
Nerve block groupBupivacaine hydrochloride 0.5% (Marcaine, Pfizer)3 point genicular nerve block under ultrasound guidance. half ml of Bupivacaine hydrochloride 0.5% (Marcaine, Pfizer) was injected in each point.
intra-articular steroid injectionBupivacaine hydrochloride 0.5% (Marcaine, Pfizer)1 mL of triamcinolone 40 milligrams (Kenacort, Bristol Myers Squip) was injected intraarticular.
intra-articular steroid injectiontriamcinolone 40 milligrams (Kenacort, Bristol Myers Squip)1 mL of triamcinolone 40 milligrams (Kenacort, Bristol Myers Squip) was injected intraarticular.
Primary Outcome Measures
NameTimeMethod
SOLAR score for inflammation changes by ultrasoundat 0 time after 2 weeks and after 12 weeks

0 means normal and 27 means the worst possible inflammation

Pain changes by VASat 0 time after 2 weeks and after 12 weeks

0 means no pain and 10 means the most severe pain

Lysholm score for change in knee functionat 0 time after 2 weeks and after 12 weeks

100 means the best performance and 0 means complete loss of function

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Minia university

🇪🇬

Minya, Egypt

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