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Homeopathic treatment of dry eyes

Efficacy of Nux moschata 6CH on tear production in patients with dry eyes in adults: A double-blind, randomized, placebo-controlled trial - NIL

Status
Recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/04/066491
Enrollment
60
Registered
2024-04-29
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Health Condition 1: H049- Disorder of lacrimal system, unspecified

Interventions

Intervention1: Nux moschata in 6CH (centesimal potency) with concomitant care: Intervention is planned as administering Nux moschata 6CH once daily for 4 weeks. Each dose will consist of 4 cane sugar

Sponsors

The Calcutta Homoeopathic Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age between 18 and 65 years. 2. Participants of either sex or transgender. 3. Participants providing written informed consent voluntarily. 4. Diagnosed dry eye disease patients using the Ocular Surface Disease Index (OSDI) questionnaire with values ranging from 13 to 32. 5. Adequate similarity with the symptomatology of Nux moschata, as decided by the homeopathic doctor

Exclusion criteria

Exclusion criteria: 1. Subjects diagnosed to have severe dry eye (OSDI greater than 32). 2. Subjects who have used contact lenses within the last 6 months. 3. Subjects who are on treatment with other artificial tear products, other topical drops or previously diagnosed with other ocular diseases. 4. Subjects with active or untreated malignancy or recovered from malignancy. 5. Vulnerable population: unconscious, non-ambulatory, too sick for consultation, differently abled, terminally or critically ill patients, mentally incompetent people. 6. Diagnosed cases of unstable mental or psychiatric illness or other uncontrolled or life-threatening illness affecting quality of life or any organ failure. 7. Pregnant and puerperal women, lactating mothers. 8. Self-reported immune-compromised state. 9. Substance abuse and/or dependence. 10. Already undergoing homeopathic treatment for chronic disease within the last 6 months. 11. Simultaneous participation in any other clinical trials.

Design outcomes

Primary

MeasureTime frame
Tear production values in both eyes using Schirmer’s test strips without the use of topical anaesthesiaTimepoint: At baseline, and every week, up to 4 weeks.

Secondary

MeasureTime frame
Participants self-administered Ocular Surface Disease Index (OSDI) questionnaireTimepoint: At baseline, and every week, up to 4 weeks.

Countries

India

Contacts

Public ContactBhiswadeb Das

The Calcutta Homoeopathic Medical College and Hospital

drkisorkumarnaskar@gmail.com9433039891

Outcome results

None listed

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