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Observational study of medical treatment for acute osteomyelitis and pyogenic arthritis

Observational study of medical treatment for acute osteomyelitis and pyogenic arthritis - Observational study of medical treatment for acute osteomyelitis and pyogenic arthritis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000054606
Enrollment
200
Registered
2024-07-01
Start date
2024-08-09
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

acute osteomyelitis, septic arthritis

Interventions

None listed

Sponsors

Tokyo Metropolitan Chidren's Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1 Diagnosed with acute osteomyelitis or septic arthritis at a single site based on fever, local symptoms, and imaging findings, or diagnosed with both acute osteomyelitis and septic arthritis. 2 Aged over 1 month and under 19 years old. 3 Those who showed treatment responsiveness* to initial treatment within 5 days after treatment initiation**. 4 Cases with no positive blood culture beyond 2 days after treatment initiation**. 5 Microorganisms identified from blood, joint fluid, and pus, with susceptibility. 6 Able to take medication orally or through tube feeding, and the drug can be absorbed from the gastrointestinal tract. *Treatment responsiveness: Determined when fever resolves and local redness, swelling, and pain improve compared to before treatment initiation. **Treatment initiation: Day 1 is considered as the day of the second administration of initial antimicrobial therapy.

Exclusion criteria

Exclusion criteria: 1 Those with causative microorganisms resistant to MRSA, PRSP, or other drug-resistant or acid-fast bacteria. 2 Those diagnosed as chronic osteomyelitis (with symptoms present for over 2 weeks before treatment initiation, etc.). 3 Those diagnosed with congenital or acquired immunodeficiency syndrome. 4 Cases of arthritis or osteomyelitis following trauma, surgery, or foreign body placement. 5 Cases of non-hematogenous arthritis or osteomyelitis due to direct extension from primary infectious foci. 6 Those who opted not to disclose information about this study and indicated refusal. 7 Others deemed unsuitable as subjects by the principal investigator.

Design outcomes

Primary

MeasureTime frame
The cure rate at 6 months from the start of treatment, meaning the absence of symptoms and signs of acute osteomyelitis and septic arthritis, and no requirement of additional antimicrobial therapy due to recurrence.

Countries

Japan

Contacts

Public ContactAki Miyashita

Tokyo Metropolitan Children's medical center Division of infectious disease

aki1002.miya1993@gmail.com042-300-5111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026