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Study on effectiveness of Kashmaryadi aschyotana for pittaj ahishyanda.

Open randomized controlled clinical trial to evaluate the efficacy of kashmaryadi aschyotana in the management of pittaj abhishyanda - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/112689
Enrollment
200
Registered
2026-06-15
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Health Condition 1: Z00-Z99- Factors influencing health status and contact with health services

Interventions

None listed

Sponsors

Yashwant ayurvedic medical college PG institute and research centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Irrespective of gender, religion, occupation and socioeconomical status patient will be selected randomly for study 2. Patient having sign and symptoms of pittaj abhishyanda

Exclusion criteria

Exclusion criteria: 1. Patient with any other ocular pathology (e.g. corneal ulcer, keratitis, scleritis, glaucoma , uveitis) 2. Ocular trauma or post surgical eye complications 3.Patient with known hypersensitivity reaction to trial or control drug or any of their ingredients. 4.Patient with chronic systemic illness.

Design outcomes

Primary

MeasureTime frame
To evaluate and compare the clinical efficacy of Kashmaryadi Aschyotana and Basifloxacin ophthalmic suspension in Pittaj abhishyanda (Acute Bacterial Conjunctivitis)Timepoint: 7days treatment with follow up on 0,3,5,7 day observation and assessment on 15th day

Secondary

MeasureTime frame
To study all ingredients and role of Kashmaryadi Aschyotana according to classical textTimepoint: 7 days treatment with follow up on 0,3,5,7 days observation and assessment on 15th day

Countries

India

Contacts

Public ContactDr Chandrashekhar Mule

Yashwant Ayurvedic medical college PG institute and research centre

drcnm05@gmail.com09175800710

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026