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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT01313871
Other study ID # P08167
Secondary ID
Status Withdrawn
Phase N/A
First received March 10, 2011
Last updated May 29, 2015
Start date August 2011
Est. completion date November 2012

Study information

Verified date May 2015
Source Merck Sharp & Dohme Corp.
Contact n/a
Is FDA regulated No
Health authority Russia: Ethics Committee
Study type Observational

Clinical Trial Summary

The study will assess the disease severity and treatment patterns of rheumatoid arthritis in Eastern European, Middle Eastern, and North African countries.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date November 2012
Est. primary completion date July 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria :

- Confirmed diagnosis of rheumatoid arthritis, preferably based upon criteria established by the American College of Rheumatology (ACR) 1987

- clinical signs & symptoms

- data obtained from previous laboratory and instrumental examination, which may include but is not limited to: Radiography, Blood tests

- Written informed consent, signed before participation in the study.

Exclusion Criteria :

- Refusal to participate in the study

- Age under 18 years

Study Design

Observational Model: Case-Only, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Merck Sharp & Dohme Corp.

Outcome

Type Measure Description Time frame Safety issue
Primary Number of participants with low, moderate, or high disease activity as assessed by the Disease Activity Score using 28 joint counts (DAS28) Day of enrollment (Day 0) No
Secondary The number of participants with rheumatoid arthritis visiting participating sites in the course of one year One year No
Secondary Number of participants with different degrees of disability as assessed by the Health Assessment Questionnaire (HAQ). Day of enrollment (Day 0) No
Secondary Number of participants treated with non-steroidal anti-inflammatory drugs (NSAIDs), disease-modifying anti-rheumatic drugs (DMARDS), corticosteroids, and/or biologics Day of enrollment (Day 0) No
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