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Effect of darvyadi eye drops in Kaphaja Abhishyanda (acute mucopurulent conjunctivitis)

An open labelled randomized controlled clinical study to evaluate the efficacy of darvyadi eye drops in the management of kaphaja abhishyanda with special reference to acute mucopurulent conjunctivitis - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/03/083322
Enrollment
60
Registered
2025-03-25
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: H100- Mucopurulent conjunctivitis

Interventions

None listed

Sponsors

Parul Institute of Ayurved
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Patients presenting with the signs and symptoms of Kaphaja Abhishyanda will be selected 2 Patients irrespective of Gender religion and socio-economic status will be included in study

Exclusion criteria

Exclusion criteria: 1 Patients not willing to participate in the study 2 Severe cases of conjunctivitis with complications like corneal ulcers trachoma dacryocystitis etc 3 Eye associated with any other inflammatory and infective ocular conditions 4 Patients with known case of Hypertension Diabetes mellitus and any major systemic illness

Design outcomes

Primary

MeasureTime frame
1.Evaluation of efficacy of darvyadi eye drops and Ciprofloxacin eye drops 2.Comparison of efficacy of darvyadi eye drops and ciporifloxacin eyedrops in the management ofkaphaj abhiushyanda with special reference to acute mucopurulent conjunctivitis 3.Reduction in redness and discharge 4.Relief from discomfort and itching sensation 5.Vision restorationTimepoint: Baseline DAY 1 DAY 8 DAY 15

Secondary

MeasureTime frame
Relief from symptoms of acute mucopurulent conjunctivitisTimepoint: 15 days

Countries

India

Contacts

Public ContactDr Ravi Shanker Pareek

Parul Institute of Ayurved

vdshalakapawar@gmail.com7057894025

Outcome results

None listed

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