NCT00903903

Brief Summary

The purpose of this study is to compare the data obtained by computer-aided quantification of the synovial perfusion in patients with arthritis using two-dimensional and three-dimensional power Doppler ultrasonography and the clinical data used to represent the degree of joint inflammation. Intra- and inter-observer reliability of this method will also be determined.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Apr 2009

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 1, 2009

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

May 15, 2009

Completed
4 days until next milestone

First Posted

Study publicly available on registry

May 19, 2009

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2010

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2010

Completed
Last Updated

May 19, 2009

Status Verified

May 1, 2009

Enrollment Period

11 months

First QC Date

May 15, 2009

Last Update Submit

May 18, 2009

Conditions

Keywords

active synovitis

Study Arms (2)

1

RA patients with at least one active synovitis

2

Non-RA patients with at least one active synovitis

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Arthritis patients who visited the Rheumatology out patient clinic in Taichung Veterans General Hospital

You may qualify if:

  • patients with at least one painful swollen peripheral joint observed by a rheumatologist, including:
  • shoulder joints
  • elbow joints
  • wrist joints
  • metacarpophalangeal (MCP) AND
  • proximal interphalangeal (PIP) joints of hands, ankle joints, subtalar joints, mid-tarsal joints, MTP and PIP joints of feet

You may not qualify if:

  • patients with active infection
  • patients with concurrent malignant disease
  • patients with a history of traumatic, septic, or cystal arthritis
  • previous joint surgery, or isotopic synovectomy within the past 12 months before the study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Taichung Veterans General Hospital

Taichung, 40705, Taiwan

RECRUITING

MeSH Terms

Conditions

Synovitis

Condition Hierarchy (Ancestors)

Joint DiseasesMusculoskeletal Diseases

Central Study Contacts

Hsin-Hua Chen, M.D.

CONTACT

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER

Study Record Dates

First Submitted

May 15, 2009

First Posted

May 19, 2009

Study Start

April 1, 2009

Primary Completion

March 1, 2010

Study Completion

March 1, 2010

Last Updated

May 19, 2009

Record last verified: 2009-05

Locations