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A COMPARATIVE STUDY ON THE EFFECT OF KARAVIRA EYE DROP WITH LAUHADI GUGGULU AND SHIGRUADI EYE DROP WITH HARIDRA KHANDA IN THE MANAGEMENT OF SIMPLE ALLERGIC CONJUNCTIVITIS

A COMPARATIVE STUDY ON THE EFFICACY OF KARAVIRA EYE DROP WITH LAUHADI GUGGULU AND SHIGRUADI EYE DROP WITH HARIDRA KHANDA IN THE MANAGEMENT OF VATAJA ABHISHYANDA (SIMPLE ALLERGIC CONJUNCTIVITIS)- AN OPEN LABELLED RANDOMISED CONTROLLED CLINICAL TRIAL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/03/032130
Enrollment
30
Registered
2021-03-18
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: H108- Other conjunctivitis

Interventions

Intervention1: Lauhadi Guggulu Karavira Eye drops : Lauhadi Guggulu (oral administration) 500 mg twice daily for 42 days + 14 days follow up Karavira Eye drops (Topical instillation) 01 drop 6 times/d

Sponsors

All India Institute of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients having the signs and symptoms of VVataja abhishyanda as given in Ayurvedic classics will be selected. Patients should be willing to participate in the trial.

Exclusion criteria

Exclusion criteria: Patients not willing for trial and follow up. Patients having complicated eye diseases and trachoma, chalazion, stye, pterygium, dacryocystitis, trichiasis etc. Patients suffering from corneal opacity, ulcers. Patients suffering from systemic disease like TB, Tumor

Design outcomes

Primary

MeasureTime frame
Improvement in signs and symptoms of Vataja abhishyanda. Timepoint: The duration of the trail will be carried out for a period of 42 days. Follow up observations ââ?¬â??14 days. Total course of the clinical trial ââ?¬â?? 56 days The patient will be assessed on -before administration of medicine, 14th day, 28th day and 42nd day.

Secondary

MeasureTime frame
Improvement in ocular health.Timepoint: The duration of the trail will be carried out for a period of 42 days. Follow up observations ââ?¬â??14 days. Total course of the clinical trial ââ?¬â?? 56 days The patient will be assessed on -before administration of medicine, 14th day, 28th day and 42nd day.

Countries

India

Contacts

Public ContactDr Narayana Bavalatti

All India Institute of Ayurveda

eyenimi@gmail.com9650715615

Outcome results

None listed

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