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A clinical study Nixoderm Tin for treating tinea corporis in adult individuals.

A prospective, randomized, double blind, two arm, comparative clinical study to evaluate the safety and efficacy of Nixoderm tin in tinea corporis infection in adult subjects. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/085118
Enrollment
40
Registered
2025-04-21
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: B354- Tinea corporis

Interventions

Intervention1: Nixoderm Tin: Product to be applied twice a day at the site of infected area, duration-30 days Dosage form : Cream Control Intervention1: Placebo: Product to be applied twice a day at

Sponsors

M/s.SC Johnson & Son Nigeria Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Male and Female participants 2.Aged between 18-65 years. 3.Diagnosed with tenia corporis infection 4.Willing to give Informed Consent. 5.Willing to complete the study assessments/questionnaires. 6.Willing to avoid usage of his/her own skin care products in controlling tenia corporis infection for at least one week before the commencement and during this study.

Exclusion criteria

Exclusion criteria: 1. Pregnancy or breast feeding. 2. Participants with the history of hypersensitivity to skin care products. 3. Participants with mild to severe anaphylaxis reaction. 4. Participants with pre existing severe systemic disease necessitating longterm medication. 5. Participants with any other concomitant skin diseases such as psoriasis eczema etc. 6. Evidence of significant uncontrolled comorbid disease which in the investigators opinion would jeopardize patient participation. 7. History of cancer, including solid tumors hematologic malignancies and carcinoma in situ. 8. Participation in the current or previous clinical trial with any approved or investigational products during the past 1 month.

Design outcomes

Primary

MeasureTime frame
1. Percentage reduction in ringworm infection from baseline to all study visits to be evaluated by following parameters: KOH preparation of fungus Dermatological Assessments Percentage reduction in itching and scaling from baseline to all study visits by Visual Analogue Scores.Timepoint: Screening, Day 15 and Day 30

Secondary

MeasureTime frame
The safety of Nixoderm Tin in tenia corporis infection from baseline to all study visits is determined by evaluating adverse eventsTimepoint: Day 0,Day 15 and Day 30

Countries

India

Contacts

Public ContactDr Ashok Godavarthi

Radiant Research Services PVT LTD.

surya.ashok@gmail.com09880999297

Outcome results

None listed

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