Comparison Effectiveness of Oral Ivermectin , 1% Permethrin Shampoo and 4% Dimeticone Liquid Gel in the Treatment of Pediculosis Capitis Among School Children in Chachoengsao Province, Thailand
NCT06332872 · Status: ACTIVE_NOT_RECRUITING · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 117
Last updated 2024-03-27
Summary
The goal of this clinical trial is to Comparison effectiveness of Oral ivermectin , 1% Permethrin shampoo and 4% Dimeticone liquid gel in the treatment of Pediculosis capitis, to assess the prevalence of lice and associated risk factors between severity groups by using questionnaire-based surveys and diagnostic tests among school children in Baan Nayao, Chachoengsao Province, Thailand.
The main questions it aims to answer are
* What is more effective between Oral ivermectin , 1% Permethrin shampoo and 4%Dimeticone liquid gel in the treatment of Pediculosis capitis in school children in Baan Nayao, Chachoengsao Province, Thailand?
* What is Prevalence and risk factors of being infected with in head lice in school and community?
* What is Side effects of Oral ivermectin , 1% Permethrin shampoo and 4%Dimeticone liquid gel?
Participants will receive three different drugs are
* oral ivermectin
* 4% Dimeticone liquid gel
* 1% Permethrin shampoo
Participants voluntarily received oral ivermectin as per medical prescription, with treatment outcomes, side effects, and satisfaction levels monitored following two treatment cycles. Those exhibiting persistent lice infestations were subsequently treated with 1% permethrin shampoo, the standard treatment, while alternatives were provided for individuals allergic to permethrin. These findings will contribute to formulating tailored, effective, and safe treatment regimens for future patients.
Conditions
- Pediculus Capitis Infestation
- Permethrin Adverse Reaction
- Dimethicone Adverse Reaction
- Permethrin Allergy
- Dimethicone Allergy
- Ivermectin
- School-age Children
Interventions
- DRUG
-
Oral Ivermectin
Oral formulation (3mg tablet) Dosage: 2 single doses of 200 mcg/kg given 7 days apart
- DRUG
-
4% dimenticone liquid gel
topical formulation (liquid gel) only 1 application
Sponsors & Collaborators
-
Phramongkutklao College of Medicine and Hospital
lead OTHER
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 6 Years
- Max Age
- 13 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2023-12-15
- Primary Completion
- 2024-03-18
- Completion
- 2024-05-31
Countries
- Thailand
Study Locations
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