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Clinical efficacy of Vortioxetine vs Escitalopram in depressive disorder

A 12-week Randomized Controlled Study to compare the antidepressant efficacy of Vortioxetine and Escitalopram in patients with depressive episode

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/07/043662
Enrollment
60
Registered
2022-07-04
Start date
Unknown
Completion date
Unknown
Last updated
2022-08-02

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

Conditions

Health Condition 1: F32- Major depressive disorder, singleepisode

Interventions

Intervention1: Vortioxetine: Vortioxetine will be started at a dose of 10 mg once daily and increased to 20 mg/day after 2 weeks. Control Intervention1: Escitalopram: Escitalopram will be started at a

Sponsors

Ahana Hospitals LLP
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients who are meeting International Classification of Diseases 10 criteria for major depressive disorder Patients who gave informed written consent.

Exclusion criteria

Exclusion criteria: Patients with other comorbid psychiatric disorder (except major depressive disorder) Patients who were having comorbid substance dependence Patients with any other medical disorder which is confounding our inclusion diagnosis

Design outcomes

Primary

MeasureTime frame
17-item Hamilton Depression Scale (HAM-D17) done at baseline, 2nd week, 4th week and 12th weeksTimepoint: 17-item Hamilton Depression Scale (HAM-D17) done at baseline, 2nd week, 4th week and 12th weeks

Secondary

MeasureTime frame
CGI- severity of illness (CGI-S) and improvement scale (CGI-I) done at baseline, 2nd week, 4th week and 12th weekTimepoint: CGI- severity of illness (CGI-S) and improvement scale (CGI-I) done at baseline, 2nd week, 4th week and 12th week

Countries

India

Contacts

Public ContactVikhram Ramasubramanian

Ahana hospitals, LLP

vikhram@ahanahospitals.in9443772233

Outcome results

None listed

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