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Clinical Trial to determine the effectiveness of Guduchi Ghanvati and Satwawajay Chikitsa in the Management of Depression

A Randomised Clinical Trial to determine the effectiveness of Guduchi Ghanvati and Satwawajay Chikitsa in the Management of Depression (Vishad) - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/11/059448
Enrollment
180
Registered
2023-11-02
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: - Health Condition 2: F339- Major depressive disorder, recurrent, unspecified Health Condition 3: F339- Major depressive disorder, recurrent, unspecified

Interventions

None listed

Sponsors

SUNDARSINGH K DANGA
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients who complain about the Depression (Vishad). Patients who are willing to give consent to participate in this study.

Exclusion criteria

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.

Design outcomes

Primary

MeasureTime frame
Response to Ayurvedic treatment (Guduchi Ghanvati as well as Satwawajay Chikitsa & also placebo) (improvement or remission in subjective or for criteria of assessment). Improvement in Quality of life within 3 months. It is Cost effective treatment. 3.Burden of disease in terms of prevalence i.e., magnitude of depression among the community. Cost effective treatment. Timepoint: Within 8 weeks

Secondary

MeasureTime frame
Withdrawals due to adverse events or lack of effectiveness or inconvenience therapy/treatment. t. Determination of Score of Hamilton Depression scaleTimepoint: after 8 weeks

Countries

India

Contacts

Public ContactARCHANA DACHEWAR

Department of Kayachikitsa, Jupiter Ayurved Medical College,Nagpur.

sunder147@gmail.com9372045685

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026