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GENetic and clinical Predictors Of treatment response in Depression

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN31345163
Enrollment
887
Registered
2003-09-19
Start date
2004-02-23
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Mental and Behavioural Disorders Mental and Behavioural Disorders Depression

Interventions

1. Reboxetine 4mg bd 2. Paroxetine 20mg

Sponsors

Medical Research Council (UK)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 18-74 years with the more severe depressions in whom the GP and patient have already agreed that antidepressants should be prescribed. We will therefore only include those with a Clinical Interview Schedule - Revised (CIS-R) score of =20, a Beck Depression Inventory (BDI) score of =15 and a diagnosis of International Statistical Classification of Diseases and Related Health Problems, tenth revision (ICD-10) depressive episode F32 and F33 (from CIS-R).

Exclusion criteria

Exclusion criteria: Pregnant and breast feeding women, patients with psychotic illness, alchohol or substance abuse problems, patients with medical contraindications to Citalopram or Reboxetine. (June 2006: Exclusion criteria were provided as follows: Potential subjects who have taken antidepressant medication within 2 weeks, who cannot complete self-administered scales, who have a psychosis or major substance or alcohol abuse. The GP will exclude anyone who has medical contraindications or in whom participation in the trial is not appropriate.)

Design outcomes

Primary

MeasureTime frame
Beck depression inventory total score (BDI) at 6 weeks adjusted for baseline BDI score.

Secondary

MeasureTime frame
Not provided at time of registration

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 29, 2026