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Scabies clinical trials

View clinical trials related to Scabies.

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NCT ID: NCT02407782 Completed - Scabies Clinical Trials

Oral Ivermectin Versus Topical Permethrin to Treat Scabies in Children and Adults

SCRATCH
Start date: January 19, 2016
Phase: Phase 3
Study type: Interventional

Scabies remains a frequent condition that affects adults and children. The aim of this study is to compare the efficacy and safety of two drug treatments against scabies in children and their close contacts. One group will apply topical permethrin 5% and the other group will receive oral ivermectin. Both groups will be treated twice, once at inclusion and the second time 10 days later. Both treatment regimens have been used widely and are safe to use.

NCT ID: NCT02254564 Completed - Scabies Clinical Trials

PCR (Polymerase Chain Reaction) Assay for Diagnosis of Sarcoptes Scabiei

Start date: October 2014
Phase:
Study type: Observational

The main objective of this study is to identify unique DNA sequences within the genome of human scabies that can be utilized to identify the parasite through PCR.

NCT ID: NCT02094716 Completed - Scabies Clinical Trials

A Dose Ranging Vehicle Controlled Study to Determine the Safety and Efficacy of Permethrin Foam, 5% and Permethrin Foam, 4% for the Treatment of Scabies

Start date: April 2014
Phase: Phase 2
Study type: Interventional

To determine and compare the safety and efficacy of permethrin foam 4% and permethrin foam 5% with that of vehicle in subjects with scabies.

NCT ID: NCT00884728 Completed - Scabies Clinical Trials

Evaluation of a Regional Healthy Skin Program in Remote Aboriginal Communities of Australia's Northern Territory

EAHSP
Start date: September 2004
Phase: N/A
Study type: Observational

The purpose of this study is to determine whether a coordinated regional approach to healthy skin programs in six remote Aboriginal communities can demonstrate, not only a reduction in the burden of scabies and streptococcal skin sores, but also broad health benefits, including primary prevention of some chronic diseases that occur at particularly high rates in Australian Aboriginal communities. The primary objectives of the Program are: - Demonstrate a reduction in scabies and skin sores on a regional basis - Demonstrate the broader public health effects of Healthy Skin Programs, particularly those relating to chronic diseases such as rheumatic fever and renal diseases - Build on the existing Indigenous capacity by assisting in the development of new knowledge and skills to improve the health and well being of Indigenous communities - Establish the feasibility of incorporating Healthy Skin Programs into existing health service delivery

NCT ID: NCT00604084 Completed - Scabies Clinical Trials

Veron Scabies Education and Eradication Program

VSEEP
Start date: May 2007
Phase: N/A
Study type: Interventional

The purpose of this project is to develop a community scabies eradication and education program for the highly endemic areas surrounding the Veron community on the eastern tip of the Dominican Republic. It proposes the use of oral Ivermectin as a replacement for topical Lindane--a readily available medical formulation, pesticide, and environmental toxin that is reported to be banned in the Dominican Republic as well as over 80 other countries throughout the world.

NCT ID: NCT00436891 Completed - Clinical trials for Streptococcus Group A

Streptococcal Infections in Fiji - Prevalence of Group A Streptococcal Pyoderma and Scabies in Infants in Fiji

Start date: February 2007
Phase: N/A
Study type: Observational

Group A streptococcus (GAS) is a bacteria that causes many different sicknesses in children and adults. This study will look at the number of cases of pyoderma (bacterial skin infection) and scabies (skin mites that cause itching) in 550 infants 12 months or younger in Fiji. (GAS can cause pyoderma, and sometimes skin sites infested with scabies can become infected with GAS bacteria.) The study will also look at the makeup of GAS and how certain medications affect GAS. The infants will be involved in the study for approximately 1 week. Their skin will be examined for pyoderma and scabies. A swab sample will be taken from the pyoderma area to test for GAS. The researchers hope to see how often these skin infections occur and how they affect the Fijian population. The information will help the researchers to develop better treatment and possibly a vaccine to prevent infection. Infants with pyoderma that is defined as "greater than mild" will be referred for treatment.

NCT ID: NCT00284843 Completed - Clinical trials for Streptococcus Group A

Prevalence of RHD, Pyoderma and Scabies in Children in Fiji

Start date: January 2006
Phase: N/A
Study type: Observational

The purpose of this study is to estimate the number of cases of rheumatic heart disease, pyoderma, and scabies in school age children in Fiji. In addition the study will describe the features of rheumatic heart disease, pyoderma, and scabies in these children. Study participants will include 5200 primary school children, ages 5-14, from 21 primary schools in the Central Division of Fiji. These children will be examined for pyoderma, scabies, and the doctor will listen to their heart with a stethoscope. Any child that has a heart murmur detected will have their heart looked at through an echocardiogram test (uses sound waves to create a picture of how the heart is working). Any child that is found to have rheumatic heart disease will be referred to a pediatric cardiologist for further evaluation. Participants will be involved in the study for about 2 days.

NCT ID: NCT00262418 Completed - Scabies Clinical Trials

Comparison of the Efficacy and Safety of Ivermectin to Permethrin

Start date: July 2004
Phase: Phase 2
Study type: Interventional

Comparison of the efficacy and safety of a single administration of ivermectin to a single administration of permethrin for the treatment of scabies