A clinical trial to study the effect of kushmanand beej churn and satvavajaya chikitsa in the patient having sign and symptoms of dhee dhriti and smriti ( manas rog)

â??An Etiopathological Study of impairment of Dhee Dhriti Smriti w.s.r. to Mild Cognitive Impairment and Therapeutic Evaluation of Kushmanda Beeja Churna and Satvavajaya Chikitsaâ??

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2019/12/022259

Enrollment

Registered

2019-12-05

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: F19- Other psychoactive substance related disorders

Interventions

Intervention1: kushmand beej churn: 6 gm BD with honey after meal Control Intervention1: KUSHMAND BEEJ CHURN: KUSHMAND BEEJ CHURN 6gm twice a day AND KUSHMAND BEEJ CHURN SATVAVAJAYA CHIKITSA Control

Eligibility

Inclusion criteria

Inclusion criteria: The Individuals having the all age group more than 18 years with impairment of Dhee, Dhriti and Smriti.

Exclusion criteria

Exclusion criteria: Schizophrenia, Parkinsonism, Dementia, Alzheimer, Uremia, Encephalopathy preganant women, lactating mother and any major systemic disorder.

Design outcomes

Primary

Measure	Time frame
patients of both sexes age group above 18 years of dhee dhriti smriti will be selected for reliving sign and symptomsTimepoint: patients of both sexes age group above 18 years of dhee dhriti smriti will be selected for reliving sign and symptoms	—

Secondary

Measure	Time frame
asses the comparative efficacy between both groups after 8 weeks in case of dhee dhriti and smriti impairment.Timepoint: asses the comparative efficacy between both groups after 8 weeks in case of dhee dhriti and smriti impairment	—

Countries

India

Contacts

Public ContactAnshu Sharma

National Institute of Ayurveda

drsksm31@rediffmail.com9414361874

Outcome results

None listed

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