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Compare the efficacy of isotretinoin and Terbinafine combination with Terbinafine alone in the treatment of recurrent fungal infections of the skin

Evaluation Of Effectiveness Of Combination Of Isotretinoin With Terbinafine And Terbinafine Alone In The Treatment Of Recurrent Dermatophytosis: A randomised Controlled Trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/11/010471
Enrollment
100
Registered
2017-11-13
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Recurrent Dermatophytosis Of Skin- Tinea Cruris and Corporis

Interventions

Intervention1: Group A: groupA- isotretinoin(0.5mg/kg) once daily and Terbinafine 250 mg twice daily for a period of 4 weeks. Control Intervention1: group B: Group B: terbinafine at 250 mg twice daiy

Sponsors

AIIMS New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Patients >= 18 years of age with tinea cruris and/or tinea corporis. 2) KOH (10%) positivity by microscopy from the lesion during the time of presentation. 3) Two or more episodes in one year. 4) Patients consenting to participate in the study.

Exclusion criteria

Exclusion criteria: 1) Not willing to consent and follow up for the study. 2) Patients who have received any topical antifungal therapy within last 2 weeks or oral antifungal therapy in the previous 4 weeks. 3) Immunocompromised patients. 4) Patients with known active liver, cardiac, renal or neurological diseases or uncontrolled diabetes Mellitus. 5) Hypersensitivity to either isotretinoin or terbinafine. 6) Pregnant and lactating women. 7) Women desiring pregnancy.

Design outcomes

Primary

MeasureTime frame
Cure rates of infection both clinically and microbiologiically in both the groupsTimepoint: After 4 weeks/ 6 weeks of treatment and after 3 months follow up

Secondary

MeasureTime frame
1) species identification 2) side effects of treatmentTimepoint: After 4 weeks/ 6 weeks of treatment and at 3 months follow up

Countries

India

Contacts

Public ContactDr Gridharan senthilnathan

All India Institute Of Medical Sciences, New Delhi

prokverma@hotmail.com01126593454

Outcome results

None listed

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