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Depression and its management by Saraswata Churna Takra-Dhara and Go Ghrita Nasya

A Clinical study of Saraswata Churna and Takra-Dhara along with Gavya Ghrita Nasya in the management of Manoavsad

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/12/016722
Enrollment
40
Registered
2018-12-19
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: F329- Major depressive disorder, singleepisode, unspecified

Interventions

Intervention1: Saraswata churna: two dose of 1gm Saraswata churna orally with 2.5ml gavya ghrita and 5ml madhu after meals for 60 days Control Intervention1: Saraswat Churna and Takra Dhara along with

Sponsors

Dr Sarvepalli Radhakrishnan Rajasthan Ayurved UniversityJodhpur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients diagnosed as per the criteria for mild and moderate depression as per BDI(Beck Depression Inventory). 2.Age between 16 to 50 years. 3.Patients of either gender,irrespective of socioeconomic status. 4.Patients with history of depression less than two year. 5.Patients who were under medication for depression previously but not using now. 6.Patients ready to sign informed consent form.

Exclusion criteria

Exclusion criteria: 1.Patients with other psychiatric disorders. 2.Depressive phase of substance abuse disorder. 3.Pregnant women. 4.Patients with suicidal tendency/thoughts. 5.Post Schizophrenic Depression. 6.Patients with Hypotension.

Design outcomes

Primary

MeasureTime frame
Improvement in subjective and objective parameterTimepoint: 2 months

Secondary

MeasureTime frame
To find the comparative efficacy of the treatments in the different groupsTimepoint: 2 months

Countries

India

Contacts

Public ContactDr Kintul Joshi

DSRRAU,Jodhpur

drpramodmishra4@gmail.com9001009793

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026