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Effect of Antidepressants on White Matter Structure

C

Centre de Recherche de l'Institut Universitaire en santé Mentale de Montréal

Status and phase

Unknown
Phase 4

Conditions

Major Depression

Treatments

Drug: Desvenlafaxine

Study type

Interventional

Funder types

Other
Industry

Identifiers

Details and patient eligibility

About

Subjects with major depression will be evaluated and intensively characterized through questionnaires, computerized cognitive evaluation and laboratory investigations. Magnetic resonance imaging will be used to document baseline white matter structure. subjects will then receive desvenlafaxine which will be adjusted as clinically indicated. After 16 weeks the evaluations will be repeated.

Full description

40 subjects will be included in the study. Diagnosis will be confirmed by MINI. Participants will be characterised using questionnaires, pain threshold, cognition, facial expression recording and MRI. Desvenlafaxine will be initiated at 50mg AM. At week 8 Desvenlafaxine may be increased to 100mg as clinically indicated. Measures will be repeated at the end of the study.

Enrollment

40 estimated patients

Sex

All

Ages

18 to 55 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Major depression
  • Age 18 to 55
  • Hamilton grater or equal to 20

Exclusion criteria

  • Major neurologic disorder
  • Major cardiovascular disorder
  • Unstable medical condition
  • Significant psychiatric co-morbidity
  • Current substance dependance
  • Pregnancy or lactation -Treatment resistance as defined by nonresponse to 2 or more antidepressant treatments (adequate dose and duration) -

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

Trial contacts and locations

1

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Central trial contact

Louise Normandeau, Nurs; souad Lahlafi, BNurs

Data sourced from clinicaltrials.gov

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