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Cardiovascular Effects of Agomelatine and Escitalopram in Patients With Major Depressive Disorder (MDD)

Information source: Baker IDI Heart and Diabetes Institute
ClinicalTrials.gov processed this data on August 23, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Major Depressive Disorder (MDD)

Intervention: Agomelatine (Drug); Escitalopram (Drug)

Phase: Phase 4

Status: Not yet recruiting

Sponsored by: Baker IDI Heart and Diabetes Institute

Official(s) and/or principal investigator(s):
Gavin Lambert, Study Director, Affiliation: Baker IDI Heart & Diabetes Institute
David Barton, Principal Investigator, Affiliation: Monash Medical Centre

Overall contact:
Sarah Tremethick, Phone: +61 3 8532 1145, Email: sarah.tremethick@bakeridi.edu.au

Summary

There is strong evidence that patients with major depressive disorder (MDD) are at increased risk of developing coronary heart disease (CHD). This elevated risk is independent of classical risk factors such as smoking, obesity, hypercholesterolemia, diabetes and hypertension. The risk of CHD is increased 1½-2 fold in those with minor depression and 3-4½ fold in subjects with MDD. Put simply, the relative risk of developing CHD is proportional to the severity of the depression. While the mechanism of increased cardiac risk attributable to MDD is not known disturbances in autonomic function most likely do play a part. In untreated patients with MDD (with no underlying CHD) the investigators have identified that a marked sympathetic nervous activation and diminished heart rate variability (HRV) occurs in a proportion (approximately one third) of patients. Diminished HRV has been linked to increased incidence rates of acute cardiac events in conditions such as hypertension, diabetes and myocardial infarction. Importantly, whether treating depression actually improves the risk of: (1) CHD development or (2) recurrence of cardiac events in patients with existing CHD remains unknown. The investigators, and others, have provided a growing body of evidence linking elevated sympathetic activity and exaggerated sympathetic responses to stress to early stages of end organ dysfunction and markers of disease development. Of particular note, in addition to possible effects on HRV is the association of chronic sympathetic nervous activation to: (a) abnormal blood pressure regulation and (b) the development of insulin resistance. The investigators therefore plan to examine the cardiovascular effects of two different antidepressant medications, agomelatine and escitalopram, in patients with MDD. In addition, the investigators plan to investigate the effects these two medications have on sympathetic nervous system activity, blood pressure, HRV, endothelial function, metabolic and psychological effects. Findings from this study will assist us to identify of biological correlates of sympathetic nervous activation which will enable us to: (1) identify those at potentially increased cardiac risk, and (2) potentially implement additional therapeutic strategies in order to reduce cardiac risk. Indeed, it is not known whether antidepressant treatment alone would be sufficient to reverse any adverse effects of sympathetic nervous activation. This study aims to answer this important clinical question.

Clinical Details

Official title: A Randomised Trial Investigating the Cardiovascular Effects of Agomelatine and Escitalopram in Patients With Major Depressive Disorder.

Study design: Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Primary outcome: Change from baseline in markers of sympathetic nervous system activity.

Secondary outcome:

Change from baseline in the magnitude of morning surge in blood pressure.

To determine the association between sympathetic nervous system activity and left ventricular hypertrophy.

Change from baseline in insulin resistance.

Change from baseline on markers of cardiac risk.

Eligibility

Minimum age: 18 Years. Maximum age: 65 Years. Gender(s): Both.

Criteria:

Inclusion Criteria:

- Aged 18-65 years.

- Capable of understanding and willing to provide signed and dated written, voluntary

informed consent in advance of any protocol-specific procedures.

- MDD or MDD with melancholia according to the Diagnostic and Statistical Manual of

Mental Disorders (DSM-IV) criteria. Patients with comorbid panic or anxiety disorders will be included if MDD is the primary diagnosis.

- Hamilton Depression (HAM D) > 18.

- Beck Depression Inventory (BDI-II) >18.

Exclusion Criteria:

- Aged < 18 or > 65 years.

- Current antidepressant treatment.

- Previous failed response to SSRI treatment at the maximum tolerated dose for at least

4 weeks.

- Known or suspected hypersensitivity to either escitalopram or agomelatine or any of

their ingredients.

- Current high suicide risk.

- Comorbid panic or anxiety disorders as the primary diagnosis.

- Pre-existing and/or current diagnosed heart disease.

- Comorbid medical conditions including type 1 diabetes, hepatic impairment (cirrhosis

or active liver disease), medicated hypertension, epilepsy, bleeding disorders, alcohol/drug dependence, infectious blood diseases, psychotic disorders, personality disorders, eating disorders, mental retardation, dementia (ie, Mini Mental State Examination [MMSE] < 23), or gastrointestinal illness or previous bariatric (weight loss) surgery that may impair antidepressant absorption.

- Participants on betablockers (for example, metoprolol).

- Participants currently taking the following contraindicated medications for

agomelatine and/or escitalopram:

- Cytochrome (CYP) P450 1A2 inhibitors (e. g. fluvoxamine, ciprofloxacin)

- Monoamine Oxidase Inhibitors;

- Irreversible non-selective monoamine oxidase inhibitors (MAOIs)

- Reversible, selective MAO-A inhibitor (e. g. moclobemide)

- Reversible, non-selective MAOI (e. g. linezolid)

- Pimozide

Participants who are eligible to take part in the study are prohibited to take the contraindicated medications listed above for the entire duration of the study.

- Clinically significant abnormalities on examination or laboratory testing and

clinically significant medical conditions not listed above that are serious and/or unstable.

- Pregnant or breastfeeding women.

- Women of childbearing potential (WOCP) who are not using medically accepted

contraception (ie, intrauterine devices [IUDs], hormonal contraceptives [oral, depot, patch or injectable], and double barrier methods such as condoms or diaphragms with spermicidal gel or foam). Women who are postmenopausal (ie, amenorrhea for at least 12 consecutive months) or surgically sterile are not considered to be WOCP.

- Sexually active men with WOCP partners who are not using medically accepted

contraception. Medically accepted contraception for women and sexually active men with WOCP partners will be continued throughout the study and for 30 days after the last antidepressant dose.

Locations and Contacts

Sarah Tremethick, Phone: +61 3 8532 1145, Email: sarah.tremethick@bakeridi.edu.au

Monash Medical Centre - Monash Health, Clayton, Victoria 3168, Australia; Not yet recruiting
David Barton, Principal Investigator
Arup Dhar, Sub-Investigator
Sarah Tremethick, Sub-Investigator
Jennifer Grigo, Sub-Investigator
Krishna Vaddadi, Sub-Investigator

Alfred and Baker Medical Unit - Alfred Hospital, Melbourne, Victoria 3004, Australia; Not yet recruiting
Gavin Lambert, Principal Investigator
Arup Dhar, Sub-Investigator
Sarah Tremethick, Sub-Investigator
Jennifer Grigo, Sub-Investigator
Markus Schlaich, Sub-Investigator
Elisabeth Lambert, Sub-Investigator
Murray Esler, Sub-Investigator
Geoff Head, Sub-Investigator
Nina Eikelis, Sub-Investigator
Carolina Ika Sari, Sub-Investigator
Petra Marusic, Sub-Investigator
Toni Rice, Sub-Investigator
Mariee Grima, Sub-Investigator
Donna Vizi, Sub-Investigator
Louise Hammond, Sub-Investigator
David Barton, Sub-Investigator
Dagmara Hering, Sub-Investigator

Baker IDI Heart & Diabetes Institute, Melbourne, Victoria 3004, Australia; Not yet recruiting
Gavin Lambert, Principal Investigator
Arup Dhar, Sub-Investigator
Sarah Tremethick, Sub-Investigator
Jennifer Grigo, Sub-Investigator
Markus Schlaich, Sub-Investigator
Elisabeth Lambert, Sub-Investigator
Murray Esler, Sub-Investigator
Geoff Head, Sub-Investigator
Nina Eikelis, Sub-Investigator
Carolina Ika Sari, Sub-Investigator
Petra Marusic, Sub-Investigator
Toni Rice, Sub-Investigator
Mariee Grima, Sub-Investigator
Donna Vizi, Sub-Investigator
Louise Hammond, Sub-Investigator
David Barton, Sub-Investigator
Dagmara Hering, Sub-Investigator

Additional Information

Starting date: January 2014
Last updated: December 16, 2013

Page last updated: August 23, 2015

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