clinical study with a combination of kushmanda swarasa and yashtimadhu in the condition of occupational stress

Clinical study on effectiveness of kushmanda swarasa with yashtimadhu churna in chittodvega

Status

Active, not recruiting

Phases

Phase 1Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2018/09/015661

Enrollment

Registered

2018-09-07

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: F40-F48- Anxiety, dissociative, stress-related, somatoform and other nonpsychotic mental disorders

Interventions

Intervention1: A single arm clinical trial with combination of Kushmanda Swarasa and Yashtimadhu churna: 100 ml kushmanda swarasa with 3g yashtimadhu churna daily on empty stomach morning hour for 30

Eligibility

Inclusion criteria

Inclusion criteria: 1.subjects between age group 20-60 years irrespective of gender and socio-economic status 2.subjects who are ready to sign the informed consent

Exclusion criteria

Exclusion criteria: 1. subjects having un controlled Diabetes Mellitus, uncontrolled Hypertension and other systemic diseases 2.subjects suffering from other psychiatric illness 3.subjects suffering from other organic brain disease 4.subjects suffering from complication of substance abuse

Design outcomes

Primary

Measure	Time frame
Cohens Perceived Stress score 30% reduced in one monthTimepoint: outcome assessed in 1 month	—

Secondary

Measure	Time frame
Reduced stress level, anxiety and apprehension 50%Timepoint: one month intervention	—

Countries

India

Contacts

Public ContactDr LakshmiA

Sri Dharmasthala Manjunatheshwara College of Ayurveda and Hospital

adiga.manjunatha@gmail.com9035715798

Outcome results

None listed

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