Comparison of Oral Ivermectin and Permethrin 5% Lotion in Treatment of Pediculosis Capitis
NCT05643820 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 60
Last updated 2022-12-09
Summary
In children, pediculosis is a common ectoparasitic infestation. Infestation of head lice (Pediculus humanus capitis) causes a variety of physical symptoms, including pruritus, excoriation, cervical lymphadenopathy, and conjunctivitis1. It also has a number of negative social consequences, including parental anxiety and stigmatization of infested children2.
It is a significant public health issue that primarily affects school-aged children aged 8 to 113. In developing nations, prevalence rates of up to 40% have been reported4. The four urban areas of KPK (NWFP) reported prevalence of 36.7%5. People with a low socioeconomic background and poor hygiene are more likely to be affected6.
Pediculosis capitis has been treated using a variety of treatment modalities. They include both physician prescription and over-the-counter medications. Permethrin or ivermectin had been used topically or orally. Permethrin is a neurotoxin that is synthesized. It is a pyrethroid neurotoxic that targets voltage-sensitive Sodium ion receptors in the neurological system of the insect, triggering nerve depolarization, hyperexcitation, muscular paralysis, and, eventually, parasite death7. Ivermectin is antiparasitic medication, it is possible to treat diseases like lymphatic filariasis, and ectoparasite infestations, primarily scabies, with ivermectin because it binds to glutamate gated chloride ion receptors of invertebrates and disrupts neurotransmission8.
The rationale of this study is to study while comparing effectiveness of oral ivermectin and topical permethrin in management of pediculosis. The topical medication usage is problematic and had reported drug resistance9. There has been less regional or national research on the effectiveness of oral Ivermectin, so doctors less frequently use it in our department. Instead, the patients are treated for pediculosis capitis with topical Permethrin.
Conditions
- Pediculosis
Interventions
- DRUG
-
Permethrin 5% topical lotion
patients in group A prescribed with 5% topical permethrin lotion two overnight applications seven days apart
- DRUG
-
Ivermectin
patients in group B and weighing more than 15 kgs were given oral ivermectin 200 microgram/kg two doses seven days apart
Sponsors & Collaborators
-
Combined Military Hospital Abbottabad
lead OTHER
Principal Investigators
-
Bushra Muzaffar, FCPS · Combined Military Hospital Abbottabad
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 8 Years
- Max Age
- 36 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2022-03-01
- Primary Completion
- 2022-08-31
- Completion
- 2022-08-31
Countries
- Pakistan
Study Locations
More Related Trials
-
Better Options for Lymphatic Filariasis Treatment
NCT07159373 ·Status: NOT_YET_RECRUITING ·Phase: PHASE3
-
Efficacy of Ivermectin in COVID-19
NCT05076253 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Moxidectin Versus Ivermectin as Mass Drug Administration for the Control of Onchocerciasis and Other Neglected Tropical Diseases
NCT07145736 ·Status: RECRUITING ·Phase: PHASE4
-
Multiple Versus Single Dose of Ivermectin for the Treatment of Strongyloidiasis
NCT01570504 ·Status: COMPLETED ·Phase: PHASE3
-
Effectiveness of Ivermectin in SARS-CoV-2/COVID-19 Patients
NCT04739410 ·Status: COMPLETED ·Phase: PHASE4
-
Efficacy and Safety of Emodepside in Adults Infected With Strongyloidiasis Stercoralis
NCT06373835 ·Status: COMPLETED ·Phase: PHASE2
-
Safety and Efficacy of Novel Combination Regimens for Treatment of Onchocerciasis
NCT06070116 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE2
-
Assessing the Safety and Efficacy of a Combination Therapy for STH in PSAC in Bangladesh
NCT07045493 ·Status: ENROLLING_BY_INVITATION ·Phase: PHASE2
-
Safety and Tolerability of a Novel Malathion Formulation in Infants and Toddlers With Head Lice
NCT00291057 ·Status: TERMINATED ·Phase: PHASE2
-
Bioavailability Pilot Study of Versus W0035 Versus Stromectol
NCT03717558 ·Status: WITHDRAWN ·Phase: PHASE1
-
Evaluation of Effectiveness of ALBENDAZOLIVERMECTIN Coformulation vs ALBENDAZOLE for Treatment of Intestinal Worms
NCT05124691 ·Status: TERMINATED ·Phase: PHASE2/PHASE3
-
Efficacy, Safety and Acceptability of Ivermectin ODT in PSAC
NCT06184399 ·Status: COMPLETED ·Phase: PHASE2
-
Efficacy of Ivermectin-albendazole vs Albendazole Alone in School-aged Children Infected With Trichuris Trichiura
NCT06037876 ·Status: COMPLETED ·Phase: PHASE3
-
Treatment of Strongyloides Infection
NCT03605758 ·Status: TERMINATED ·Phase: PHASE3
-
Co-administration of IVM and ALB in School-based Deworming in Uganda
NCT06497075 ·Status: COMPLETED
-
A Pharmacokinetic and Safety Study of Moxidectin to Identify an Optimal Dose for Treatment of Children 4 to 11 Years
NCT03962062 ·Status: COMPLETED ·Phase: PHASE1
-
Effectiveness of Combined Albendazole and Ivermectin Treatment for Intestinal Worm Infections
NCT00207753 ·Status: COMPLETED ·Phase: NA
-
Comparative Efficacy of Different Mebendazole Polymorphs in the Treatment of Soil-transmitted Helminth Infections
NCT01350271 ·Status: COMPLETED ·Phase: PHASE3
-
The Effect of a Deworming Intervention to Improve Early Childhood Growth and Development in Resource-poor Areas
NCT01314937 ·Status: COMPLETED ·Phase: PHASE4
-
Efficacy of Higher Albendazole and Ivermectin Doses on Wuchereria Bancrofti Microfilarial Clearance in Malawi
NCT01213576 ·Status: TERMINATED ·Phase: NA
-
A Study to Assess the Efficacy and Safety of Mebendazole for the Treatment of Helminth Infections in Pediatric Participants
NCT02034162 ·Status: COMPLETED ·Phase: PHASE3
-
Efficacy and Safety of IVM/ALB Co-administration
NCT03527732 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
Testing Insect Repellents Against Musca Sorbens, the Vector of Trachoma
NCT03813069 ·Status: COMPLETED ·Phase: PHASE2
-
Azithromycin - Ivermectin Mass Drug Administration for Skin Disease
NCT02775617 ·Status: COMPLETED ·Phase: PHASE4
-
Ivermectin Versus Albendazole for Chronic Strongyloidiasis
NCT00765024 ·Status: COMPLETED ·Phase: PHASE3