CTRI/2014/03/004453
Recruiting
Phase 4
A randomized study of the cost effectiveness and tolerability of escitalopram and desvenlafaxine in treatment of moderate to severe depression
Moulya Nagraj0 sites60 target enrollmentTBD
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Health Condition 1: null- moderate depression
- Sponsor
- Moulya Nagraj
- Enrollment
- 60
- Status
- Recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Subjects of either gender aged between 18\-65 years.
- •Subjects with first episode or recurrent episode of depression according to (ICD\-10\) with baseline score \>18 and \< 40 according to MADRS.
- •Willingness to give written informed consent and available for follow up.
Exclusion Criteria
- •Atypical depression
- •Postpartum depression
- •Pregnant women, breast feeding and women planning to conceive.
- •Subjects with severe depression requiring ECT and with high risk of suicidal tendency.
- •Co\-morbid psychiatric illnesses
- •Previous history of epilepsy and sexual dysfunction
- •Serious or uncontrolled medical illness like glaucoma, hypertension, diabetes mellitus, hyperlipidemia, myocardial infarction, hepatic and renal impairment.
- •Depression secondary to medical illnesses, post traumatic depression.
- •Known history of allergy to both the study medications.
- •Participation in any other research study in recent past
Outcomes
Primary Outcomes
Not specified
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