MedPath

Study on Antidepressant Effect of Two Antidepressants Amitriptyline and Fluoxetine in patients with depressio

Phase 4
Completed
Conditions
Health Condition 1: null- depression
Registration Number
CTRI/2017/11/010443
Lead Sponsor
svasanth
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
80
Inclusion Criteria

1.19years â?? 60 years of age both sex

2.newly diagnosed patients with clinical depression (moderate to severe ) according to ICD 10 criteria

3. Major depressive disorder patients.

Exclusion Criteria

1.Less than 19 years

2. more than 60 years.

3.Pregnant and Lactating mothers.

4.Patients with h/o Cardiac , Hepatic and renal disease ,Co morbid illness and terminal illness.

Known case of Pulmonary Tuberculosis, HIV/AIDS, Leprosy, Hypothyroidism.

Patients with history of hypersensitive reaction to Amitriptyline and Fluoxetine.

Patients on any other investigational drugs.

Depression with psychosis, bipolar depression .

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
17- point HAM-D (Hamilton Depression) rating scaleTimepoint: 4 months
Secondary Outcome Measures
NameTimeMethod
17- point HAM-D (Hamilton Depression) rating scaleTimepoint: 6 months
© Copyright 2025. All Rights Reserved by MedPath