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Trial of Pindolol Augmentation in Venlafaxine Treated Patients With Major Depression

A Short Term Double Blind Randomised Trial of Pindolol Augmentation in Venlafaxine Treated Patients With Major Depression

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00159146
Enrollment
31
Registered
2005-09-12
Start date
2002-08-31
Completion date
2007-09-30
Last updated
2007-12-27

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

Conditions

Major Depression

Keywords

Major Depression, Pindolol, Venlafaxine, Augmentation, Major depression (DSM-IVR)

Brief summary

This study investigates the hypothesis that pindolol can accelerate the response to antidepressants in patients with major depression treated with venlafaxine.

Detailed description

Antidepressant therapy has a delayed onset of action of 4-6 weeks. Pindolol has in some studies shown an accelerating effect. In this study we investigate the effect of 20 mg of pindolol retarded formulation in combination with Venlafaxine compared to placebo Pindolol and Venlafaxine for a duration of 19 days. Effect is measured by the Hamilton Depression rating Scale and the Preskorn Scale (self-rating).

Interventions

DRUGPindolol and venlafaxin

pindolol 20 mg and venlafaxin 150 mg

Sponsors

Wyeth is now a wholly owned subsidiary of Pfizer
CollaboratorINDUSTRY
Tvergaards Foundation
CollaboratorUNKNOWN
Hillerod Hospital, Denmark
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

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

Inclusion criteria

* Major depression

Exclusion criteria

* Allergy towards pindolol, venlafaxine or other tablet constituents * Liver or kidney impairment * Diabetics * Age below 18 years * Severe cardiac disease * Asthma.

Design outcomes

Primary

MeasureTime frame
Hamilton Depression Rating Scale scores1 week

Secondary

MeasureTime frame
Preskorn scoresone day

Countries

Denmark

Outcome results

None listed

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