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COMPARATIVE CLINICAL STUDY BETWEEN LASHUNA AND SHATAVARI IN MINIMIZING THE RISK OF POSTMENOPAUSAL OSTEOPOROSIS

COMPARATIVE CLINICAL STUDY BETWEEN LASHUNA AND SHATAVARI IN MINIMIZING THE RISK OF POSTMENOPAUSAL OSTEOPOROSIS

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/04/008407
Enrollment
30
Registered
2017-04-24
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: null- postmenopausal osteoporosis

Interventions

Intervention1: Lashuna tablets: DOSE 6 gms per day in 3 divided doses DOSAGE FORM Tablet (500mg) ANUPANA Milk ROUTE Oral duration 12 weeks Control Intervention1: Shatavari tablets: 6 gms per day in 3

Sponsors

PARUL INSTITUTE OF AYURVEDA
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: -Women of age group 40-60 years (Perimenopausal ,Menopausal, Post Menopausal age group) presentingoneormore risk factors ofdevelopingOsteoporosis. -Clinical symptoms of Osteoporosisand laboratoryinvestigations showing boneloss. -OsteoporoticfemalepatientswhoseBMD(t-score)isequaltoorlessthan-1willbe taken forthe present study. - Patients diagnosedto beOsteoporoticon the basisof Singhâ??sindex. - Patients presenting with the classical symptoms of Asthi Kshaya vis-a-via Osteoporosiswillbetaken for the study.

Exclusion criteria

Exclusion criteria: BMD â??tâ?? â??score above -1 will be excluded. • Patients suffering from neoplasm of the bone will be excluded. • Known cases of Diabetes mellitus, uncontrolled Hypertension, Thyrotoxicosis, Hyper Parathyroidism, Addisonâ??s disease, Pagetâ??s disease, Cushingâ??s syndrome, Tuberculosis of the bone, Osteomalacia, and Chronic Renal, Hepatic and Cardiac Failure will be excluded. • Rheumatoid Arthritis, Gouty Arthritis and any long-standing systemic disorder will be excluded.

Design outcomes

Primary

MeasureTime frame
reduces the post menopausal riskof osteoporosisTimepoint: reduces the post menopausal riskof osteoporosis

Secondary

MeasureTime frame
reduce pain,improves the quality of lifeTimepoint: 12 weeks

Countries

India

Contacts

Public ContactDR MANSI MODI

Parul Institute Of Ayurveda

mansi.modi1@gmail.com9979883317

Outcome results

None listed

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