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Better Disease Control by Multidrug Regimen in Scabies

B

B.P. Koirala Institute of Health Sciences

Status

Completed

Conditions

Scabies

Treatments

Drug: Permethrin Lotion 5% and Oral Ivermectin 200 mcg/kg
Drug: Permethrin Lotion 5%

Study type

Interventional

Funder types

Other

Identifiers

NCT05198947
162/073/074-IRC

Details and patient eligibility

About

Scabies is associated with significant discomfort and social taboo. Existing treatment regimen frequently fails due to lack of patient compliance. We compared single use regimen to existing standard repeat application regimen for treatment of scabies.

Enrollment

212 patients

Sex

All

Ages

5 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Willing patients
  • Clinical diagnosis of scabies
  • Within the age limits

Exclusion criteria

  • Unwilling patients
  • Patients with severe co-morbidities requiring long term medication
  • Pregnant women
  • Patients who don't fulfill the age limit criteria

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

212 participants in 2 patient groups

Group 1 Permethrin only
Active Comparator group
Description:
Standard regimen of permethrin 5% topical application to be repeated after 1 week.
Treatment:
Drug: Permethrin Lotion 5%
Group 2 Permethrin and Ivermectin
Active Comparator group
Description:
A combination regimen of permethrin 5% topical application with oral ivermectin 200 mcg/kg given on the single day only
Treatment:
Drug: Permethrin Lotion 5% and Oral Ivermectin 200 mcg/kg

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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