Skip to content

Individualised Homoeopathy compared with Artificial tear drops in management of mild to moderate Dry Eye Disease

A prospective three arm randomised pilot trial to evaluate the role of individualised Homoeopathy compared with Artificial Teardrops in managing mild to moderate dry eye disease DED. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/091588
Enrollment
192
Registered
2025-07-24
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Health Condition 1: H041- Other disorders of lacrimal gland

Interventions

Intervention1: Individualised Homoeopathic medicines : Homoeopathic drugs as detailed in the standard Homoeopathic Materia Medica and in the Homoeopathic Pharmacopoeia (India/US) will be used in the

Sponsors

Central Council for Research in Homoeopathy
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Male or female patient aged 18 years or above. Presenting with at least two of dry eye related symptoms, including itching, dryness, foreign body sensation, burning, blurred vision, photophobia, and soreness or pain etc in at least one of the eye. Diagnosis of mild to moderate dry eye syndrome with or without Sj grens syndrome. Best corrected visual acuity 6/18. Following results in at least one of the eye Ocular Surface Disease Index OSDI test symptoms between 12 and 33 Tear film break up time less than or equal to 10 seconds in atleast one of the eye. Willing to follow the study schedule and provide written informed consent

Exclusion criteria

Exclusion criteria: 1 Complaints of ocular comorbidity including non-dry eye ocular inflammation, severe blepharitis, glaucoma, contact lens allergy or any condition known to have effect on the study outcome. 2 History of any Trauma or eye surgery during last 3 months 3 Presenting with any uncontrolled systemic disease or significant illness and other autoimmune or connective tissue disorders such as rheumatoid arthritis and lupus, and thyroid disease. 4 Current use of topical ophthalmic medications that could affect dry eye syndrome and not willing to stop. 5 Pregnant &/or lactating female or considering a pregnancy.

Design outcomes

Primary

MeasureTime frame
Change in Ocular Surface Disease Index OSDI score Change in intensity of symptoms of dry eye disease on VAS self-assessment of ocular discomfort reported by participants Timepoint: Baseline, monthly for 06 months

Secondary

MeasureTime frame
-Change in tear film break-up time -Change in Tear osmolarityTimepoint: Baseline and end of treatment at 06 months

Countries

India

Contacts

Public ContactDr Subhash Kaushik

Central Council for Research in Homoeopathy

dr.deepti.2821@gmail.com9818785593

Outcome results

None listed

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