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Management of Molluscum with Homoeopathy medicine

Management of Molluscum Contagiosum with Individualized Homoeopathy A Single Blind Randomized Placebo Controlled Trial - NIL

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/088337
Enrollment
220
Registered
2025-06-05
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Health Condition 1: B081- Molluscum contagiosum

Interventions

Intervention1: Individualized Homoeopathic medicine: Individualized homoeopathic remedies in centesimal potencies and appropriate doses will be prescribed for oral administration based on symptom simi

Sponsors

Central Council for Research in Homoeopathy, New Delhi, Ministry of AYUSH, Government of India
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients having age between 2-25years. 2.Patients of both sexes. 3.Patients presenting with characteristic features of molluscum including firm, pearly, dome-shaped papules with central umbilication (pit); pink or skin colored lesions which may be symptomatic or asymptomatic. These lesions can be itchy or painful and may appear individually or in groups. 4.Having at least three lesions of molluscum 5.Participant is willing to participate in the study and give written consent/assent for the study

Exclusion criteria

Exclusion criteria: 1.Patients on conventional treatment or other systems of medicine for the symptoms of molluscum contagiosum. 2.Immunocompromised patients. 3.Pregnant or breastfeeding females. 4.Patients with significant injury on and/or surrounding MC that may impact ability to treat and count lesions 5.Molluscum associated with active cases of atopic dermatitis 6.Patients suggestive of sexually transmitted molluscum contagiosum

Design outcomes

Primary

MeasureTime frame
1.Changes in cases of molluscum using Investigator and Subject Global Severity Assessment, Investigator and Subject Global Impression of Change score. 2. Changes in BOTE score of inflammationTimepoint: 1.From baseline, fortnightly till 12 weeks (end of treatment). 2.From baseline, fortnightly till 12 weeks (end of treatment).

Secondary

MeasureTime frame
1.Changes in overall life quality of cases of molluscum using CDLQI in children and DLQI in adults 2.Changes in number of molluscum lesion Timepoint: 1.From baseline, every month of treatment till the end of the treatment. (3rd month) 2.From baseline, fortnightly till 12 weeks (end of treatment)

Countries

India

Contacts

Public ContactDr Renu Mittal

Central Council for Research in Homoeopathy

dr.ritikanarula@gmail.com09811281206

Outcome results

None listed

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