To examine the effect of Karanja Beeja Varti Anjan application in 84 participants (both male and female) of age group between 18 to 55 years with signs of progressive pterygium.

Randomized controlled clinical study to evaluate the efficacy of Karanja Beej Varti Anjan in Prastari Arma with special reference to Progressive Pterygium - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/03/083268

Enrollment

Registered

2025-03-24

Start date

Unknown

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: H110- Pterygium of eye

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Patients having Lakshanas of Aushadhi Sadhya Arma. Patients with pterygium type I extending up to 2mm on the cornea.

Exclusion criteria

Exclusion criteria: Patients with pterygium and associated with other ocular conditions will be excluded from study. Patients with Chhedya and Asadhya arma will be excluded. Those who are suffering from serious illness like Cardiac Disorders, HIV, TB, Leprosy,Cancer, Diabetes mellitus, Asthma, Renal Impairments, Hepatitis and those who are on Immune Suppressive drugs will be excluded from the study. Pregnant and nursing mothers are excluded from study.

Design outcomes

Primary

Measure	Time frame
To evaluate the effectiveness of Karanja Beej Varti Anjan in Prastari Arma.Timepoint: 21 days	—

Secondary

Measure	Time frame
Adverse reaction if any.Timepoint: 21 days	—

Countries

India

Contacts

Public ContactDr Manasi Surendra Karjini

LKR Ayurvedic Mahavidyalaya Post Graduate Training and Research Center, Gadhinglaj, Kolhapur

ayurraga@gmail.com9972616774

Outcome results