CTRI/2022/10/046915
Not yet recruiting
Phase 2
Comparative evaluation of clinical anxiolytic efficacy of Sitadi Agada and Imipramine (TCAs) in the management of Generalized Anxiety Disorders (GAD)- A reverse Pharmacology approach.
I0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- I
- Status
- Not yet recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •a)Patient willing to sign the consent form.
- •b)Patients of either sex with age between 18 to 60 years.
- •c)Patient fulfilling the Diagnostic and Statistical Manual of Mental Disorder, Fourth Edition (DSM â?? IV).
- •e)Patient who score at least 14 on the Hamilton Anxiety Rating Scale (HARSâ?? A) at baseline visit.
Exclusion Criteria
- •a)Patient who suffers Anxiety due to direct physiological effect of a substance (e.g. alcohol etc) or a general medical condition (e.g. Hyperthyroidism).
- •b)Occurrence of anxiety exclusively during mood disorder, a psychotic disorder or a pervasive development disorder.
- •c)Patients having history of chronic diseases like Diabetes Mellitus, Ischemic Disease, Dyslipidemia, Hypertension, Malignancies, Chronic Renal Failure,
- •Any Endochrinological disorders etc. will be excluded.
- •d)Patients who have completed participation in any other clinical trial during the past six months.
- •e)Pregnant or lactating women.
- •f)Any other condition which the investigator thinks may jeopardize the study.
- •g)Patients receiving Anxiolytic Drugs will be excluded.
Outcomes
Primary Outcomes
Not specified
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