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Study Evaluating Venlafaxine Extended Release in Elderly Depressed Patients

Vandral Retard (Venlafaxine Extended Release) in Depressive Syndrome With Anxiety and Painful Symptoms in Elderly Patients. Observational Study in Primary Care

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00247429
Enrollment
59
Registered
2005-11-01
Start date
2004-07-31
Completion date
2005-10-31
Last updated
2009-09-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Depressive Syndrome

Keywords

depression, anxiety, elderly

Brief summary

In this study we will assess as a primary objective the effect of venlafaxine retard treatment on primary care attended elderly patients with depressive syndrome. We will also study secondarily its effects on anxiety, somatic and painful symptoms of depression.

Interventions

None listed

Sponsors

Wyeth is now a wholly owned subsidiary of Pfizer
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients older than 60 years * Depressive syndrome with associated anxiety symptoms, according to a symptoms intensity HAM-D17³14

Exclusion criteria

* Participation in other studies in the last 3 months before the start of the study * Known hypersensibility to venlafaxine * Clinically significant abnormalities according to the venlafaxine labeling

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026