To study Keshghana Karma Of Mashi

â??A Comparative Pharmacetico-Analytical and Clinical study of Shami Mashi prepered by Open and Closed method W.S.R to its Keshagna Karmaâ??

Status

Active, not recruiting

Phases

Phase 1Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2019/01/017337

Enrollment

Registered

2019-01-31

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

None listed

Interventions

Intervention1: Shami mashi: Dose-2gm frequency of rout of administration-local aplication at Anterior Tibial region total duation therapy - 7 days

Eligibility

Inclusion criteria

Inclusion criteria: 1.female volunteers 2.age:18-50 years 3.Gender: Female 4.Who willing to written and informed consent selected irrespective of religion & occupation and economic status. Only those female who have never under worm waxing over the Anterior Tibial Region will be selected

Exclusion criteria

Exclusion criteria: 1.Volunteers with history of hypersensitivity of skin. 2.Suffering from any skin disease. 3.Diagnosed as sever systemic disease

Design outcomes

Primary

Measure	Time frame
To study pharmaceutico - analytical and clinical efficacy of Shami Mashi.i.e keshgna karmaTimepoint: 2 gm for 7 days 1 od half hr	—

Secondary

Measure	Time frame
To study pharmaceutico - analytical and clinical efficacy of open and closed method Shami Mashi.i.e keshgna karmaTimepoint: 2 gm for 7days od half hr	—

Countries

India

Contacts

Public ContactDrMinakshi Harishchandre

College of Ayurvedic Research Center,Akurdi

sharadabedade6656@gmail.com8329305483

Outcome results