CTRI/2012/08/002895CompletedPhase 4
Assessment of efficacy and safety of desvenlafaxine versus escitalopram in major depressive disorder with symptoms of anxiety:a randomized clinical trial
Department of Pharmacology IPGMER Kolkata0 sites85 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Phase 4
- Status
- Completed
- Sponsor
- Enrollment
- 85
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •subjects of major depressive disorder with symptoms of anxiety with HAM score of seven to eighteen
- •baseline HAMA score more than or equal to twelve
- •Subjects must be willing to give written informed consent
Exclusion Criteria
- •subjects with age less tha eighteen or more than sixty
- •Pregnant and lactating women
- •Baseline HAMD score less than seven or more than eighteen
- •Baseline HAMA score less than 12
- •Subjects with psychotic features
- •Subjects with suicidality catatonic features
- •Subjects on any antidepressant medications in the last two months
- •Subjects with concurrent severe medical disorders like uncontrolled diabetes hypertension ischemic heart disease chronic renal failure cirrhosis any malignancy etc
- •Subjects with history of substance abuse in the last two years
- •Subjects with mixed depression and anxiety disorder or any other episodes of other mood disorder bipolar disorder dysthymia etc
- •Subjects with any other psychiatric disorders
- •Subjects on other concurrent medications known to have drug interact with the study medications like other SSRI SNRI tricyclic antidepressants etc
- •Subjects with past history of anaphylaxis or hypersensitivity to any of the study medications
Investigators
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