None listed
Conditions
Interventions
Intervention1: Anutaila: AFI, Part-I, 8:1
Dose: 2 drops/day/dose/ nostril for 3 months
Control Intervention1: Not applicable: Routine diet and lifestyle
Sponsors
Central Council for Research in Ayurvedic Sciences
Eligibility
Inclusion criteria
Inclusion criteria: i Women are of scheduled Caste community in the age group 18 to 65 years ii Participants willing to provide written informed consent and participate in the study for 3 months
Exclusion criteria
Exclusion criteria: i Pregnant women women who are planning for conception lactating women ii Participants with known history or a confirmed or suspected diagnosis of Cardiac diseases Autoimmune diseases cancer and Acute inflammatory conditions iii. Known case of mental disorder like bipolar depression, Schizophrenia etc. iv. Participants who are suffering from chronic diseases and under multiple drug regimen. v. Participants with addictions to alcohol, marijuana etc. vi. Any other condition which PI may think can jeopardize the study.
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| Change of Health status assessed through Ayurveda Swasthya Assessment Scale (SAS)Timepoint: At base line and at the end of 3 months | — |
Primary
| Measure | Time frame |
|---|---|
| Change in Quality of Life assessed through WHO-QOL BREFTimepoint: At Base line, at completion of 3rd month | — |
Countries
India
Contacts
Public ContactDr Kishor Gavali
Central Council for Research in Ayurvedic Sciences
Outcome results
None listed