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To Study the Effect Of Ketakyadi Taila In Asthigata Vata correlated with Osteoporosis

A Randomized Controlled Clinical Study Of Efficacy Of Ketakyadi Taila In Asthigata Vata w.s.r. To Osteoporosis

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/04/024466
Enrollment
176
Registered
2020-04-03
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: E58- Dietary calcium deficiency

Interventions

Intervention1: Ketakyadi Taila: Ketakyadi Tail 5 ml BD mix with food for 35 days in 88 patients Control Intervention1: Tab New Bone Active: Tab New Bone active will be given 1 BD after food for 35 day

Sponsors

Dr Ardra Bhagwatrao Thorat
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.BMD less than or equal to -2.5 2.If diabetic patients BSL random less than 200mg /dl 3.BMR less than 25

Exclusion criteria

Exclusion criteria: 1.Patients having any congenital bone disease 2.Patients having tuberculosis, endocrinal disease,any malignancies, bone tumor,other metabolic bone disease 3.Patients taking or require Hormone therapy 4.Patients taking steroidal therapy 5.Patients immediately require any surgical interventions for their bone and joint disease 6.Any complication arises during the treatment or if any patient discontinue the treatment will be rejected 7.ANC and PNC female

Design outcomes

Primary

MeasureTime frame
To study the efficacy of Ketakyadi Taila in Asthigata Vata w.s.r. to Osteoporosis Timepoint: 35 days

Secondary

MeasureTime frame
1.To study probable mode of action of Ketakyadi taila 2.Bone mineral density changes and symptomatic relief to the patients Timepoint: 1,2,3,4,5 Weeks up to 35 days

Countries

India

Contacts

Public ContactDr Ardra Bhagwatrao Thorat

Tilak Ayurved Mahavidyalaya

drnvborase@gmail.com9422032696

Outcome results

None listed

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