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Clinical Trials/CTRI/2022/10/046915
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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional

Investigators

Sponsor
I

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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