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Clinical Trials/NCT01219686
NCT01219686
Terminated
Phase 2

Antidepressant Effect of Escitalopram: Delay of Onset. Clinical Randomized Double-blinded Study With Three Parallel Treatment Groups (Escitalopram 20mg vs Escitalopram 30mg vs Escitalopram 20 mg + Pindolol 15 mg/Day

Markus KOSEL1 site in 1 country18 target enrollmentOctober 2010

Overview

Phase
Phase 2
Intervention
escitalopram, pindolol
Conditions
Unipolar Depression
Sponsor
Markus KOSEL
Enrollment
18
Locations
1
Primary Endpoint
MADRS score change between baseline and 2 weeks of treatment
Status
Terminated
Last Updated
10 years ago

Overview

Brief Summary

The main purpose of this study is to determine whether the antidepressant response of escitalopram 30mg/day or escitalopram 20mg/day + pindolol, a beta blocker, is different (faster) compared to a standard dose of escitalopram 20mg/day.

Detailed Description

Antidepressant drug therapy is the primary therapeutic treatment option in moderate to severe Major Depressive Disorder. However, clinically significant antidepressant response needs sustained treatment during weeks to months. Indeed, in the largest effectiveness study conducted to date (STAR\*D study) involving nearly 3000 depressed outpatients, only about one third of those who ultimately responded did so after 6 weeks of drug treatment and for most patients longer treatment periods were necessary. This delay implies prolonged suffering for the patients and their families. By its antagonist action on the serotonin 1A receptor pindolol is hypothesized to reduce the down-regulation mechanisms of antidepressants. It is therefore expected that addition of pindolol to escitalopram will shorten the therapeutic response. Clinical and preclinical data indicate that escitalopram at 30 mg/day might be more effective and perhaps be associated with a faster onset of action than 20mg. For this purpose the speed of action will be compared between three blindly randomized samples: * escitalopram 20mg per day + placebo * escitalopram 30mg per day + placebo * escitalopram 20mg per day + pindolol 15mg per day (two doses of 7.5mg during 14 days). Subjects will be followed for 6 weeks. The dose of 15mg pindolol per day (during 14 days) is based on the optimal occupancy of the serotonin 1A receptor. At inclusion all subjects will be assessed by a trained psychiatrist using the SCID I mood disorder part which is based on DSM IV criteria, and by means of the French version of the MINI. Severity of depression will be assessed using the MADRS clinician rated and self-report questionnaire, and the French version of the QIDS. Each week subjects will be assessed using the two versions of the Montgomery-Asberg Depression Rating Scale (MADRS) and the HCL-32 a self-report questionnaire assessing hypomania. It is planned to include 135 patients during the three years of the study duration resulting in 45 subjects in each group.

Registry
clinicaltrials.gov
Start Date
October 2010
End Date
June 2013
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Markus KOSEL
Responsible Party
Sponsor Investigator
Principal Investigator

Markus KOSEL

MD-PhD

University Hospital, Geneva

Eligibility Criteria

Inclusion Criteria

  • patients aged between 18 and 65 years old
  • patients suffering from major depression according to DSM-IV with a MADRS score of at least 25 and not treated by an antidepressant at the time of inclusion with the exception of non-responders to antidepressant for a period of at least 6 weeks or not tolerating an ongoing antidepressant necessitating a change of the antidepressant(excluding fluoxetine and irreversible MAOI)
  • informed consent
  • Exclusion criteria:
  • any other Axis I disorder excluding anxiety disorder not dominating the clinical picture, nicotine abuse
  • non-responders to escitalopram in the past
  • already taking pindolol
  • pregnancy and breast feeding
  • contraindication to one of the two treatments (medical conditions, drug treatments)
  • significant somatic comorbidity interfering with the study procedures

Exclusion Criteria

  • Not provided

Arms & Interventions

escitalopram 20mg + pindolol 15mg

Days 1-2: escitalopram 10 mg + placebo, days 3-42: escitalopram 20mg + placebo Days 1-14: pindolol 15 mg, days 15-17: pindolol 7.5 mg

Intervention: escitalopram, pindolol

Escitalopram 30 mg

Days 1-2: escitalopram 10 mg+ placebo, days 3-4 escitalopram 20 mg + placebo, days 5-42: escitalopram 30mg+ placebo

Intervention: escitalopram

escitalopram 20 mg

days 1-2: escitalopram 10 mg+ placebo, days 3-42: escitalopram 20 mg + placebo

Intervention: escitalopram

Outcomes

Primary Outcomes

MADRS score change between baseline and 2 weeks of treatment

Time Frame: day 14

Differences in MADRS score changes (baseline-day 14) between treatment groups

Secondary Outcomes

  • Adverse events(See primary outcome measure)
  • Correlation of drug level of pindolol and/or escitalopram and clinical outcome (primary outcome) between treatment groups(Day 10)
  • Response/remission (MADRS) at 6 weeks(day 42)

Study Sites (1)

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