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Comparison of Desipramine – Serteraline – Venlafaxine in Major Depression Disorder of Patients with Alzheimer Disease

Comparison of Desipramine – Serteraline – Venlafaxine in Major Depression Disorder of Patients with Alzheimer Disease

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201108165280N6
Enrollment
60
Registered
2013-02-28
Start date
2011-06-10
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Major Depression. Severe depressive episode without psychotic symptoms

Interventions

Intervention 1: The starting dose will be 25 mg/d serteralin -during the next month this dose gradually will reach to 150mg/d serteralin. Intervention 2: The starting dose will be 25 mg/d desipramine
Treatment - Drugs
The starting dose will be 25 mg/d serteralin -during the next month this dose gradually will reach to 150mg/d serteralin.
The starting dose will be 25 mg/d desipramine -during the next month this gradually dose will reach to 150mg/d desipramine.
The starting dose will37.5 mg/d bevenlafaxin, during the next month this dose gradually will reach to 150mg/d for venlafaxine.

Sponsors

Mashhad University of Medical Scinces
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: the patients or their family sign informed consent; Approving Mild To Moderate Alzheimer Disease Using Dsm?-TR Criteria By Psychiatrist; Out Patient Treatment; No Other Medication Except : H2 blockers – Anti Hypertensive Or Other Cardiovascular Drugs And Medications For Hypercholestrolemia. Exclusion Critera: Any Psychotropic Drugs (Except Achetyl – Aceterase Inhibitor ) During Last 2 Weeks; Substance Abuse; Any Other Psychiatric Illness; side effects of medication during study; the patient decided to leave the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Depression. Timepoint: weeks 2-4-8-12. Method of measurement: HRSD (Hamilton rating scale depression).

Secondary

MeasureTime frame
Mental Status. Timepoint: weeks 0,2,4,8,12. Method of measurement: Minimal Mental Status Examination (MMSE).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Ebrahim Abdollahian

Ibn-e-sina hospital, Mashhad University of Medical Scinces

Abdollahiane@mums.ac.ir+98 51 1711 2701

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026