Skip to content

Do Antidepressants Induce Metabolic Syndromes METADAP Study

Do Antidepressants Induce Metabolic Syndromes

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00526383
Acronym
METADAP
Enrollment
624
Registered
2007-09-10
Start date
2007-11-30
Completion date
2013-04-30
Last updated
2014-04-17

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

Conditions

Major Depressive Disorder

Keywords

Major depressive disorder, Antidepressants, Weight gain, Metabolic syndromes

Brief summary

Since antidepressants and antipsychotics have common receptorial mechanisms of action (H1 antagonism, 5HT2 antagonism), the impact of antidepressants in terms of metabolic syndromes is a matter of concern. The main objective of this study is to assess the differential impact of antidepressants in terms of weight gain and metabolic syndromes.

Detailed description

Since antidepressants and antipsychotics have common receptorial mechanisms of action (H1 antagonism, 5HT2 antagonism), the impact of antidepressants in terms of metabolic syndromes is a matter of concern. The main objective of this study is to assess the differential impact of antidepressants in terms of weight gain and metabolic syndromes. Prospective 6-month naturalistic cohort study, comparing 4 classes of antidepressants (SSRIs, SNRIs, TCAs and others) to a control group (ECT and r-TMS), in 600 patients with a major depressive disorder requiring the beginning of either antidepressant or ECT/r-TMS treatment.

Interventions

DRUGTricyclic antidepressants

antidepressant version medical dispositive

Sponsors

Institut National de la Santé Et de la Recherche Médicale, France
CollaboratorOTHER_GOV
Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Age : 18-70 * Current major depressive episode (Major depressive disorder) based on the MINI interview * HAM-D \>18 * Requiring either antidepressant treatment, either ECT or r-TMS (as assessed by the clinician) * Signed informed consent

Exclusion criteria

* Bipolar disorder (DSM-IV), Psychotic disorder (DSM-IV), Substance abuse or dependence (DSM-IV) * Normothymic treatment * Antipsychotic treatment

Design outcomes

Primary

MeasureTime frame
Definition criteria of the metabolic syndromes: Weight and waist circumference Systolic and diastolic blood pressure Glycemia Triglyceridemia Cholesterolemia Insulinemiaat Months 0, 1, 3, 6

Secondary

MeasureTime frame
Antidepressant efficacy (HAM-D, quickIDS-C, quickIDS-SR, CGI)at Months 0, 1, 3, 6

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026