None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Female subjects 30-60 years of age will be included.2.Female subjects with no history of allergy to oils.3.Be willing to refrain from taking any medication during or before the study for the said indication. 4.An ambulatory female subject can provide verbal and written consent and is ready to comply with all study procedures.
Exclusion criteria
Exclusion criteria: 1. Female subjects with Depression, Social phobias, Hypertension, Cardiac diseases, Epilepsy, Asthma, Hyperthyroidism, Alcoholics, and Drug addicts 2. History of psychiatric disorder that may impair the ability of subjects to provide written informed consent.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. To study the efficacy of Panchakarma Essential in female patients with generalized anxiety disorders. 2. To study the changes in the Visual analogue & mood assessment scores. Timepoint: 7 sittings once a week (i.e. for 2 months) | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess the improvement in the Quality of life of a patientTimepoint: 7 sittings once a week (i.e. for 2 months) | — |
Countries
India
Contacts
Mprex Healthcare Pvt. Ltd.