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Prevention of cartilage destruction in rheumatoid arthritis by etanercept (PRECEPT study)

Prevention of cartilage destruction in rheumatoid arthritis by etanercept (PRECEPT study) - PRECEPT study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000001798
Enrollment
100
Registered
2009-03-25
Start date
2008-07-01
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

Rheumatoid arthritis

Interventions

Injection of etanercept by 50 mg/week for one year Injection of etanercept by 25 mg/week for one year

Sponsors

Team RA, Rheumatosurgery, Osaka City University Medical School
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All patients must have active rheumatoid arthritis at enrollment with requirements that they have more than 4 swollen joints or more than 4 tender joints (using a 68-joint count). The elevations in the level of C reactive protein or erthrocyte sedimentation rate are not required. DAS(disease activity score)28 must be over 3.2 or patients must desire the use of biologics when DAS28<3.2.

Exclusion criteria

Exclusion criteria: Cases who have Joint destruction on hand and foot, in whom we can't measure modified Sharp score. Except Eetanercept dose, there is no restriction for other medicine use.

Design outcomes

Primary

MeasureTime frame
Total Sharp score (erosion and joint space narrowing)

Countries

Japan

Contacts

Public ContactTatsuya Koike

Osaka City University Medical School Rheumatosurgery

tatsuya@med.osaka-cu.ac.jp06-6645-3984

Outcome results

None listed

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