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Comparative outcome in different dosage of intra-articular steroid injection for symptomatic osteoarthritis of hip, a randomized control trial of multicenter study

Comparative outcome in different dosage of intra-articular steroid injection for symptomatic osteoarthritis of hip, a randomized control trial of multicenter study

Status
Unknown
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20220301001
Enrollment
130
Registered
2022-03-01
Start date
2022-03-14
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Hip osteoarthritis Hip steroid injection Hip osteoarthritis

Interventions

injection of 20 mg triamcinolone acetonide intra-articular of osteoarthritis hip under fluoroscopic controlled,injection of 40 mg triamcinolone acetonide intra-articular of osteoarthritis hip under fl
Experimental Drug,Active Comparator Drug
20mgHI,40mgHI

Sponsors

Thai Orthopedic Society for Sports Medicine (TOSSM)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. primary and secondary osteoarthritis of hip in Tonnis classification 1-3 with failure conservative treatment more than 4 weeks. (If bilateral involvement, evaluated the main site or injection site) 2. age between 40-80 years 3. no history of previous hip surgery 4. no history of hip injection within 1 year before enrollment 5. understand well in Thai language and can made self-decision

Exclusion criteria

Exclusion criteria: 1. uncontrolled and poor-controlled diabetic mellitus 2. history of infection around the hip joint 3. osteonecrosis of hip 4. Inflammatory hip arthritis such as Ankylosing Spondylitis, Sero-Negative Spondyloarthropathy, rheumatoid arthritis 5. allergy to anesthetic agents or steroid 6. pregnancy (by history taking if LMP) 7. history of degenerative spine disease with significant radicular pain or neurological deficit 8. evidence of osteolytic or osteoblastic lesion around the hip 9. planning for hip replacement within 6 months

Design outcomes

Primary

MeasureTime frame
EQ5D-VAS 2, 6 , 12, 18, 24 weeks 0-100 scale,HOOS 2, 6 , 12, 18, 24 weeks scale,mHHS score 2, 6 , 12, 18, 24 weeks scale

Secondary

MeasureTime frame
VAS pain 2, 6 , 12, 18, 24 weeks 0-10 scale

Countries

Thailand

Contacts

Public ContactAdinun Apivatgaroon

Thammasat University

adino_ball@yahoo.com66819592752

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026