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Role of Escitalopram Add-on in schizophrenia having subsyndromal depressive symptoms

A study of Escitalopram Add-on in patients with stable schizophrenia having subsyndromal depressive symptoms

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/01/011551
Enrollment
66
Registered
2018-01-24
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- STABLE SCHIZOPHRENIA

Interventions

Intervention1: escitalopram: escitalopram is an antidepressant Control Intervention1: Escitalopram and placebo: Escitalopram 10mg 1HS for 8 weeks Placebo 1 capsules 1HS for 8 weeks

Sponsors

Pooja Singh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Patients aged between 18 to 50 years. 2)Availability of a reliable informant. 3)Written informed consent from the patient and/or informant. 4)Diagnosis of Schizophrenia as per ICD-10, DCR. 5)Satisfying operational definition of stable schizophrenia. 6)Having SSDs as defined for the purpose of this study

Exclusion criteria

Exclusion criteria: 1)Patients having clinically significant medical disorder / disability or taking treatment for same. 2)Any comorbid psychiatric disorder other than nicotine dependence. 3)Patients already receiving antidepressants or mood stabilisers during last 8 weeks. 4)Patients who have received electroconvulsive therapy, other somatic treatments or any form of Psychotherapy during the last six months. 5)Any significant abnormality in routine investigations at baseline (Hb, TLC, DLC, RBS, S.Urea, S.Creatinine, LFT) 6)Pregnant and lactating females.

Design outcomes

Primary

MeasureTime frame
PANSS, HAM-D, SOFAS, SCoRSTimepoint: at 8 weeks

Secondary

MeasureTime frame
PANSS, SOFAS, HAM-D, SCoRSTimepoint: 4 WEEKS

Countries

India

Contacts

Public ContactPooja Singh

KGMU, LUCKNOW

an.kgmu@gmail.com7860001001

Outcome results

None listed

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