Clinical Trial to determine the effectiveness of Guduchi Ghanvati and Satwawajay Chikitsa in the Management of Depressio
Phase 2
- Conditions
- Health Condition 1: - Health Condition 2: F339- Major depressive disorder, recurrent, unspecifiedHealth Condition 3: F339- Major depressive disorder, recurrent, unspecified
- Registration Number
- CTRI/2023/11/059448
- Lead Sponsor
- SUNDARSINGH K DANGA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients who complain about the Depression (Vishad).
Patients who are willing to give consent to participate in this study.
Exclusion Criteria
1.Known cases and taking treatment for bipolar disorders, Schizophrenia, Psychosis, and mental retardation.
2.Patients having any type violent behaviours known by relative.
3.Patients who have taken part in any other clinical trial related to mental disorders.
1.Known cases and taking treatment for bipolar disorders, Schizophrenia, Psychosis, and mental retardation.
2.Patients having any type violent behaviours known by relative.
3.Patients who have taken part in any other clinical trial related to mental disorders.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Response to Ayurvedic treatment (Guduchi Ghanvati as well as Satwawajay Chikitsa & also placebo) (improvement or remission in subjective or for criteria of assessment). <br/ ><br>Improvement in Quality of life within 3 months. It is Cost effective treatment. <br/ ><br>3.Burden of disease in terms of prevalence i.e., magnitude of depression among the community. <br/ ><br>Cost effective treatment. <br/ ><br>Timepoint: Within 8 weeks <br/ ><br>
- Secondary Outcome Measures
Name Time Method Withdrawals due to adverse events or lack of effectiveness or inconvenience <br/ ><br>therapy/treatment. <br/ ><br>t. <br/ ><br>Determination of Score of Hamilton Depression scaleTimepoint: after 8 weeks