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DECT and MRI study of knee osteoarthritis

DECT and MRI study of knee osteoarthritis

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900024305
Enrollment
Unknown
Registered
2019-07-05
Start date
2017-08-01
Completion date
Unknown
Last updated
2019-07-15

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

Conditions

Osteoarthritis

Interventions

Gold Standard:Clinical outcome: 1.Recurrent episodes of genual arthralgia for one month
2. X-ray shows asymmetric arthrostenosis, subchondral bone sclerosis and (or) cystic degeneration, and osteophytes of the joints
3. Synovial fluid is clear and viscous, and the WBC<2000ml
4. Morning stiffness<=30min
6. Bone friction sounds when&#
Index test:DECT and MRI

Sponsors

The First Affiliated Hospital of University of South China
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. aged >=40 years; 2. Those who voluntarily participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. With history of knee trauma or surgery; 2. Mandatory spondylitis, rheumatoid arthritis, reactive arthritis, psoriatic arthritis or severe visceral lesions, severe metabolic disorders and bone tumors; 3. Those who had received immunosuppressant, adrenocortical hormone or systemic therapy before the trial; 4. Contraindications for MRI examination; 5. Poor image quality.

Design outcomes

Primary

MeasureTime frame
bony and soft tissue structures of the knee;

Countries

China

Contacts

Public ContactHeng Zhao

The First Affiliated Hospital of University of South China

angerh9@126.com+86 18974735009

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026