None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Women who have attained menopause Able to take the drug orally and comply with study procedures;
Exclusion criteria
Exclusion criteria: In shock, Consumption of other oral probiotic supplements during the trial; Patients with severe underlying diseases that affects survival, including uncontrolled malignant tumor with multiple metastases that cannot be resected, Blood diseases, Dyscrasia, Active bleeding, Severe malnutrition Patients allergic to systemic enzyme supplements; Patients facing imminent death in the opinion of the clinical team; Patients with Hb less than 10 g/dl; Patients who have participated in any other clinical study within 2 weeks prior to randomization
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in score of MENQOL (Menopause-Specific Quality of Life) questionnaire after a 6-week supplementation of ShatavariTimepoint: 6 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| NILTimepoint: NIL | — |
Countries
India
Contacts
AIIMS Bibinagar