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To study the effects of permethrin and ivermectin in patients with scabies.

A Comparative study to evaluate Efficacy and Safety of Topical Permethrin versus Oral Ivermectin in patients with scabies at a tertiary care centre: A Randomised controlled study. - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/11/076913
Enrollment
110
Registered
2024-11-18
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

Health Condition 1: L088- Other specified local infections of the skin and subcutaneous tissue

Interventions

Intervention1: Permethrin cream: Two times topical application of five percent permethrin cream once a week Control Intervention1: Tab Ivermectin: Tab Ivermectin 12mg oral route 2 tablets once a week.

Sponsors

Dr Anitha
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients willing to give written informed consent 2. Patients of either sex aged 18 to 60 years 3. Patients diagnosed with uncomplicated scabies

Exclusion criteria

Exclusion criteria: 1. Patients with crusted scabies, secondary infections and its consequences like skin sores, septicemia, heart disease, chronic kidney disease. 2. Patients with history of epileptic fits, immunodeficiency and any other coexisting skin disease that could interfere with treatment evaluation. 3. Pregnant and lactating mothers 4. In addition, patients with history of known hypersensitivity to Ivermectin. 5. Psychiatric/ emotional disturbance in patients which could limit ability of patients to comply.

Design outcomes

Primary

MeasureTime frame
Efficacy will be assessed by : Clinical improvement in signs and symptoms such as, 1.Measuring reduction in the Pruritus with skin rash at week 1 and 2 2.Measuring reduction in skin lesions (change in the size, number and morphology) at week 1 and 2 Safety will be assessed by: Number and severity of adverse events.Timepoint: Efficacy will be assessed by : Clinical improvement in signs and symptoms such as, 1.Measuring reduction in the Pruritus with skin rash at week 1 and 2 2.Measuring reduction in skin lesions (change in the size, number and morphology) at week 1 and 2 Safety will be assessed by: Number and severity of adverse events.

Secondary

MeasureTime frame
nilTimepoint: nil

Countries

India

Contacts

Public ContactDrGeetha A

Bangalore medical college and research institute bangalore

geethaanantharamaiah@gmail.com9886224085

Outcome results

None listed

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