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Effects of Erand mul arka eye drop on simple allergic conjunctivitis.

Randomized controlled trial of Eranad mul arka eye drop with Olopetadine 0.1% eye drop in Vataj Abhishand W.S.R simple allergic conjunctivitis.

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/05/042345
Enrollment
60
Registered
2022-05-02
Start date
Unknown
Completion date
Unknown
Last updated
2022-05-30

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

Conditions

Health Condition 1: H103- Unspecified acute conjunctivitis

Interventions

None listed

Sponsors

Vivek P Harne
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Both male and female 2) Between the age group of 18 to 60 yrs will be included in the study. 3) Patient suffering from Toda (pricking pain), Sangharsh (foreign body sensation), Vishushk Bhav (dryness feeling), Shishirasruta (cline/watery discharge), Alpashopha (mild chemosis) will be selected irrespective of their sex, education, socio economic status & religion.

Exclusion criteria

Exclusion criteria: 1) Patient not willing for trial 2) Pregnant & lactating women. 3) Patient who need surgical and other in intervention.

Design outcomes

Primary

MeasureTime frame
to see effect of Erand Mul Arka Eye drop and Olopetadine 0.1 % Eye drop in Vataj Abhi Shyand (simple allergic conjunctivitis) To review ancient literature on Vataj Abhi Shyand (simple allergic conjunctivitis) Timepoint: 7th and 15th days

Secondary

MeasureTime frame
evidence base support for the effect of Erand Mul Eye Drop as mentioned in our ancient literature provide simple and effective treatment for Vataj Abhi Shyand (simple allergic conjunctivitis) Timepoint: throught study for 15 days

Countries

India

Contacts

Public ContactVivek P Harne

Dr D Y Patil College Of Ayurveda And Research Center

pallavibhor78@gmail.com8983535924

Outcome results

None listed

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