FindTrial
Sign In

Study on Pitta prakopa in Sharad ritu with Patranga phanta

An Open label single arm clinical study on pitta prakopa in sharad ritu with patranga(Caesalpinia Sappan Linn) phanta by applying samanya vishesha siddhanta

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/10/021501
Enrollment
30
Registered
2019-10-01
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: Patranga phanta: Patranga phanta in a dose of 30 ml three times in a day after food for 15 days Control Intervention1: NIL: NIL

Sponsors

Sri Dharmasthala manjunatheshwara College of ayurveda and hospital Hassan
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Subjects between age group of 15-40 years Subjects of both genders Subjects with the features of pitta prakopa Subjects willing to participate in the study and who are ready to sign the informed consent form

Exclusion criteria

Exclusion criteria: Subjects who are not able to follow the prescribed treatment subjects with any systemic disease subjects under medication for any other disease Pregnant and Lactating woman

Design outcomes

Secondary

MeasureTime frame
To study the relation of sharad ritu and pitta prakopaTimepoint: 15 days—

Primary

MeasureTime frame
To clinically evaluate effect of patranga in pitta prakopaTimepoint: On First day and 15th day of treatment—

Countries

India

Contacts

Public ContactDr Subrahmanya Bhat

Sri Dharmasthala manjunatheshwara College of ayurveda and hospital

ayurchetan@gmail.com8884849477

Outcome results

None listed

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