A clinical study to evaluate the effciency of indigenous Avaleha formulation in the management of Rajonivrutti lakshnas w.s.r to post menopausal syndrome.
Phase 1
- Conditions
- Health Condition 1: N951- Menopausal and female climactericstates
- Registration Number
- CTRI/2019/10/021722
- Lead Sponsor
- Parul Institute of Ayurved
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Back ache
vaginal dryness
hot flushes
excessive sweating
headache
mood swings
depression
sleep disturbance
Exclusion Criteria
pre mature menopause(before 40 years)
any pre-exisiting psychological disorders
delayed menopause
diabetes mellitus
surgical menopause
disc problem
any systemic disorders
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method improvement in symptoms clinical features of post menopausal syndromeTimepoint: 3 month
- Secondary Outcome Measures
Name Time Method improvement in general health <br/ ><br> improvement in symptomsTimepoint: after clinical trial period
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie Avaleha's efficacy in alleviating menopausal symptoms like hot flashes and osteoporosis?
How does the Avaleha formulation compare to standard hormone replacement therapy in managing post-menopausal syndrome outcomes?
Are there specific biomarkers that correlate with improved response to Avaleha in patients with Rajonivrutti Lakshana Menopause?
What adverse events are associated with long-term use of Avaleha in post-menopausal women, and how are they managed?
What are the potential synergistic effects of combining Avaleha with other Ayurvedic compounds for menopausal symptom relief?