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NCT Number: NCT07247630

Comparison of Permethrin-Based Treatment Strategies Against Scabies in Infants and Young Children

To compare the efficacy of different permethrin-based therapies for scabies infestations in infants and young children.

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Key information

Age range

1 month–4 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

Pak emirates military hospital,Rawalpindi

Rawalpindi, Punjab Province, 00666, Pakistan

About this study

Globally, Scabies infects 300 million people each year and among children of developing countries, its prevalence is estimated to be about 5-10%.In Pakistan, Scabies accounts for 38% of dermatological diseases. Males are more prone to infestation than females, and early school- aged children are the most vulnerable as it is usually transmitted by prolonged skin-skin contact.

It was more widespread in urban than in rural areas with a distinct seasonal pattern, with the biggest infestation occurring in the winter and the lowest in the summer with all risk factors accounting for 89% of the variation in its prevalence.The classic scabies symptoms include an erythematous papular eruption, burrows, and intense itching with a predilection for fingers, axilla, elbows, waist, belly, groin, genital area, etc. Several antiscabietic treatment options exist, including topically applied permethrin, benzyl benzoate (BB) and crotamiton, and oral ivermectin.5 Repeated administration of topical permethrin 5%, topical BB 10-25% or systemic ivermectin dosed at 200 μg/kg body weight is currently recommended as first-line treatment by the 2017 European guidelines for the management of scabies.Permethrin, a synthetic pyrethroid with scabicidal and ovicidal activity, disrupts the function of the voltage-gated sodium channels in the neuronal membrane of the mites, resulting in paralysis and death. Permethrin is highly effective against scabies and well- tolerated without major side-effects, as it is minimally absorbed through the skin and rapidly eliminated, thus exerting minimal systemic presence in humans.Hence, it is recommended as a first-line therapy for adults and children in many countries

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 1 month to 4 years age.
  • Both gender
  • Scabies as defined in operational definition

Exclusion criteria

  • • Drug sensitivity test results for hypersensitivity to permethrin
  • Having renal or hepatic impairment.
  • Individuals with additional long-term skin and systemic disorders (such as diabetes, hypertension, asthma, epilepsy, acne, psoriasis)

Treatment and study plan

Permethrin 5%

Drug

permethrin application

Primary outcomes

  1. Treatment of scabies

    Time frame: 15 days

    For efficacy, we will see microscopy (presence of any one by examine skin scraping under a microscope for mites(eyeless and spherical in shape with eight legs parasite)/eggs (oval shape).The absence of these will be considered significant.

Secondary outcomes

  1. Scabies

    Time frame: 15 days

    Absence of burrows on skin

  2. Scabies

    Time frame: 15 days

    Absence of pruritus

Study contacts

Contact information is provided by the study sponsor or research team.

Shanza zafar, MBBs

CONTACT

[email protected]

+923425316096

Sponsors and collaborators

Lead sponsor

College of Physicians and Surgeons Pakistan

Other

Registry information

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Nov 25, 2025
Registry last updated
Feb 3, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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