Study Evaluating Rhapsody Registry in Patients With Depression and Anxiety
NCT00241397
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- Outpatient must be at least 18 years of age
- Consulting a General Practitioner for painful physical symptoms
- Written informed consent
- 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
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Descriptive Information | |||||||
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Brief Title | Study Evaluating Rhapsody Registry in Patients With Depression and Anxiety | ||||||
Official Title | An Observational Study on the Presence of Depression and/or Anxiety Disorder in Patients Consulting the General Practitioner With Painful Physical Symptoms in Belgium and Luxemburg. | ||||||
Brief 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. | ||||||
Detailed Description | Not Provided | ||||||
Study Type | Observational | ||||||
Study Design | Observational Model: Defined Population Time Perspective: Other | ||||||
Target Follow-Up Duration | Not Provided | ||||||
Biospecimen | Not Provided | ||||||
Sampling Method | Not Provided | ||||||
Study Population | Not Provided | ||||||
Condition |
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Intervention | Not Provided | ||||||
Study Groups/Cohorts | Not Provided | ||||||
Publications * | Not Provided | ||||||
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. | |||||||
Recruitment Information | |||||||
Recruitment Status | Completed | ||||||
Enrollment | 2560 | ||||||
Original Enrollment | Same as current | ||||||
Study Completion Date | Not Provided | ||||||
Primary Completion Date | Not Provided | ||||||
Eligibility Criteria | Inclusion Criteria:
Exclusion Criteria:
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Sex/Gender |
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Ages | 18 Years and older (Adult, Older Adult) | ||||||
Accepts Healthy Volunteers | No | ||||||
Contacts | Contact information is only displayed when the study is recruiting subjects | ||||||
Listed Location Countries | Belgium | ||||||
Removed Location Countries | |||||||
Administrative Information | |||||||
NCT Number | NCT00241397 | ||||||
Other Study ID Numbers | 0600B1-102003 | ||||||
Has Data Monitoring Committee | Not Provided | ||||||
U.S. FDA-regulated Product | Not Provided | ||||||
IPD Sharing Statement | Not Provided | ||||||
Responsible Party | Not Provided | ||||||
Study Sponsor | Wyeth is now a wholly owned subsidiary of Pfizer | ||||||
Collaborators | Not Provided | ||||||
Investigators |
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PRS Account | Wyeth is now a wholly owned subsidiary of Pfizer | ||||||
Verification Date | March 2007 |