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Not yet recruitingNCT06896929not existedUpdated Apr 20, 2025

Comparison of Permethrin and Ivermectin in Children Greater Than 6 Yrs Age for Treatment of Scabies

A Phase 2 interventional study of Permethrin Cream, 5% and Permethrin Cream, 5% in Scabies, sponsored by Children Hospital and Institute of Child Health, Lahore. Not yet recruiting at 1 site in Pakistan. Open to participants aged 6 Years to 15 Years. Per ClinicalTrials.gov, last updated 2025-04-20.

Sponsored by Children Hospital and Institute of Child Health, Lahore · Phase 2, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Apr 2026, 7 months ago, but the record still lists the study as not yet recruiting.
Phase
Phase 2
Study type
Interventional
Enrollment
90
Allocation
Randomized
Ages
6 Years to 15 Years
Sex
All
01

Study summary

Scabies is highly contagious,pruritic infestation of skin.Various treatment modalities have been used but search for ideal scabicide is ongoing.we wnt to coduct this study to compare the outcome of permethrin verses ivermectin in children for treatment of scabies .This randomized clinical trial will be done in children hospital lahore for 12 months.Sample size of 90 cases;30 in each group will be included through non probability consecutive sampling.Then patient will be randomly divided into 3 groups.In group A patient will be given 5% permethrin topical application to whole body single application. In Group B ,patients will be given topical permethrin for twice application 24 hrs appart ,In group C patients will be given Tablet Ivermectin single dose 200microgram/kg.Then patients will be examined after 2 weeks and 4 weeks for no of lesions and pruritis and cure will be labeled.All this information will be recorded on performa .Data will be entered and analysed by using SPSS version 26.Three groups will be compared for cure by using chi-square test.P value less than and equal to 0.05 will be considered as significant.

02

Conditions studied

  • Scabies

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Keywords

  • Comparison of permethrin and ivermectin in scabies
03

In context

Scabies

51 studies on the registry are indexed under Scabies; 10 are open to participants now.

This study's planned enrollment of 90 is below the median of 183 across 41 interventional studies indexed under Scabies.

Browse Scabies studies →

Lead sponsor

Children Hospital and Institute of Child Health, Lahore is the lead sponsor of 10 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
6 Years to 15 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age 6-15
  • Both genders
  • Diagnosed with scabies (as per operational definition)

Exclusion criteria

Exclusion Criteria:

  • Children with recurrent scabies on medical record
  • Known allergy to ivermectin or permethrin.
  • Widespread eczema or impetigo.
  • Liver dysfunction or renal failure
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
90 participants (estimated)

Study arms

  • Experimental
    Group A

    Group A will be given Permethrin

    Drug: Permethrin Cream, 5%

  • Experimental
    Group B

    Group B will be given Permethrin 5% cream twice application

    Drug: Permethrin Cream, 5%

  • Experimental
    Group C

    Group C will be given Tab Ivermectin

    Drug: Ivermectin 200 µg/kg

Interventions

  • DrugPermethrin Cream, 5%

    Permethrin 5% cream will be given as a single application

  • DrugPermethrin Cream, 5%

    Permethrin Cream will be given as twice application

  • DrugIvermectin 200 µg/kg

    Drug page: Ivermectin

    Group C will be given Tab Ivermectin

06

What researchers measure

Primary outcomes

  1. Cure of scabies.

    Cure will be labeled if greater han 50% reduction in no of lesions and pruritis observed after 4 weeks of treatment.

    Time frame: 12 months

07

Study locations

1 site
08

References and documents

Related links

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 20, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06896929
Lead sponsor
Children Hospital and Institute of Child Health, Lahore
Responsible party
Sadaf Wazir (DR SADAF WAZIR, Children Hospital and Institute of Child Health, Lahore) — Principal investigator
First posted
Mar 26, 2025
Start date
May 1, 2025 (estimated)
Primary completion
Apr 1, 2026 (estimated)
Completion
Apr 1, 2026 (estimated)
Last update
Apr 20, 2025

Study contacts

Sadaf Wazir, MBBs
Contact
sadaffahad302@gmail.com
97403284231293

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2024. You cannot join it, but the record below documents what was studied.

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Discussion

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Studies of the drug tested here: Ivermectin

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