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To See The Effect Of Sarvatobhadra Varti Anjana In Prastari Arma That Is Progressive Pterygium

Randamized Controlled Clinical Trail To Evaluate The Efficacy Of Sarvatobhadra Varti Anjana In Prastari Arma With Special Reference To Progressive Pterygium - Nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/071273
Enrollment
60
Registered
2024-07-25
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Sponsors

Dr Nikhita Shivkumar Pise
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Patient which shows symptoms of Prastari Arma. 2 Patient age group 30-60 yrs. 3 Pterygium, both from inner and outer canthus. 4 Pterygium limited to scleral part up to limbus. 5 Patient irrespective of sex, educational status, socio economic status, marital status, caste etc.

Exclusion criteria

Exclusion criteria: 1 Any acute infective ocular disease. 2 Recently operated eye. 3 Pterygium encroaching cornea. 4 Patient having major complicated systemic and eye disease.

Design outcomes

Primary

MeasureTime frame
To Study The Efficacy Of Sarvotobhadra Varti Anjana In The Management Of Prastari Arma With Special Reference To Progressive Pterygium.Timepoint: 30 Days Study With Follow Up On 7th, 14th, 21st And 30th Day

Secondary

MeasureTime frame
1. To Study In Detail The Literature About Prastari Arma. 2. To Study In Detail The Literature About Progressive Pterygium. 3. Preparation Of Sarvatobhadra Varti. 4. Analysis Of Sarvatobhadra Varti.Timepoint: 30 Days Study With Follow Up On 7th, 14th, 21st And 30th Day

Countries

India

Contacts

Public ContactDr Sunil Walvekar

LRP Ayurvedic Medical College And Hospital, PG Institute And Research Centre Islampur.

sunilwalvekar99@gmail.com9822442719

Outcome results

None listed

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