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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00241397
Other study ID # 0600B1-102003
Secondary ID
Status Completed
Phase N/A
First received October 17, 2005
Last updated March 14, 2007
Start date November 2005

Study information

Verified date March 2007
Source Wyeth is now a wholly owned subsidiary of Pfizer
Contact n/a
Is FDA regulated No
Health authority Belgium: Institutional Review Board
Study type Observational

Clinical Trial Summary

The purpose of this study is to assess the prevalence of Major Depression and/or Anxiety Disorder in patients consulting the General Practitioner with acute or chronic painful physical symptoms and to identify risk factors.


Recruitment information / eligibility

Status Completed
Enrollment 2560
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Outpatient must be at least 18 years of age

- Consulting a General Practitioner for painful physical symptoms

- Written informed consent

Exclusion Criteria:

- Patient is unable to understand and comply with procedures of the study

- Patient is unable to complete the patient ratings

- Patient has an acute pain with an obvious cause

Study Design

Observational Model: Defined Population, Primary Purpose: Screening, Time Perspective: Cross-Sectional


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Wyeth is now a wholly owned subsidiary of Pfizer

Country where clinical trial is conducted

Belgium, 

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