Determining the Complete Protection Time of an Insect Repellent With 30% Citriodiol® Against Three Species of Ticks.
NCT03708120 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 70
Last updated 2019-11-13
Summary
This study evaluates the length of time an insect repellent product can protect against three species of ticks. Participants will have one arm treated with the repellent, and throughout the next 10 hours, ticks will be given the opportunity to crawl up the treated arm. The test will stop after 10 hours or when the repellent stops working whichever occurs sooner.
Conditions
- Tick Bites
Interventions
- OTHER
-
Citrepel (Insect Repellent) EPA Reg. No. 84878-2
Citrepel (Insect Repellent) EPA Reg. No. 84878-2 is a pump spray formulation containing the active ingredient Citriodiol®, a tradename for Oil of Lemon Eucalyptus (OLE, Chemical Abstracts Service (CAS) No.: 1245629-80-4). Citriodiol® is derived from Eucalyptus citriodora leaves and contains a minimum of 65% p-Menthane-3,8-diol (PMD, CAS: 42822-86-6) and other constituents occurring naturally in the essential oil source material. The repellent is manufactured by Citrefine International Ltd and will be supplied by them in the pump spray bottle the manufacturer intends to use when the product is marketed with instructions for use on the product label.
Sponsors & Collaborators
-
ARCTEC
lead INDUSTRY
Principal Investigators
-
James G Logan · ARCTEC
Study Design
- Allocation
- NA
- Purpose
- BASIC_SCIENCE
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2018-11-15
- Primary Completion
- 2019-10-18
- Completion
- 2019-10-18
Countries
- United Kingdom
Study Locations
More Related Trials
-
A Phase 4, Randomised Vaccination Study in Healthy Adults to Investigate the Effects of Acellular Pertussis Vaccine on Colonisation With Bordetella Pertussis Using Controlled Human Infection
NCT06903221 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE4
-
MAPS & ITEC Cohorts: 6-8 Years Follow-up
NCT03763630 ·Status: COMPLETED ·Phase: PHASE2
-
Persistency Study After aP / Tdap Booster Vaccines in Adult Subjects (V113_01 Extension 1)
NCT02382913 ·Status: COMPLETED ·Phase: PHASE1
-
Phase III Randomized, Double-Blind, Placebo-Controlled Study of Acellular and Whole-Cell Pertussis Vaccines
NCT00004800 ·Status: COMPLETED ·Phase: PHASE3
-
Tdap Vaccination for Infant Caregivers
NCT01233401 ·Status: COMPLETED
-
Pertussis Vaccine in Healthy Pregnant Women
NCT00707148 ·Status: COMPLETED ·Phase: PHASE1
-
Safety and Immunogenicity Study of Tetanus, Diphtheria and Acellular Pertussis (Tdap) Vaccine
NCT02813486 ·Status: UNKNOWN ·Phase: PHASE1/PHASE2
-
Phase III Randomized, Double-Blind, Placebo-Controlled Study of Acellular and Whole-Cell Pertussis Vaccines
NCT00004799 ·Status: COMPLETED ·Phase: PHASE3
-
Immunogenicity and Safety of Booster Dose of BoostrixTM Polio Vaccine in Previously Boosted Adults
NCT01323959 ·Status: COMPLETED ·Phase: PHASE4
-
Efficacy and Safety of a Purified Standardised Wasp Venom Preparation
NCT00263926 ·Status: COMPLETED ·Phase: PHASE3
-
Safety and Immunogenicity of GSK's Tdap Vaccine (Boostrix) in Adults Aged 19 to 64 Years
NCT00346073 ·Status: COMPLETED ·Phase: PHASE3
-
Adsorption of Cell-free Diphtheria and Tetanus (Three-component) Combined With Vaccine Phase III Clinical Trial
NCT07112144 ·Status: RECRUITING ·Phase: PHASE3
-
Study of Adacel® Vaccine Administered to Persons 10 Years of Age
NCT01311557 ·Status: COMPLETED ·Phase: PHASE4
-
Adult Study to Evaluate Placement of Tympanostomy Tubes In-office (ADEPT)
NCT03197558 ·Status: COMPLETED ·Phase: PHASE2
-
Post-licensure, Modified Double-blind, Multi-center Study Evaluating Safety and Immunogenicity of ADACEL® and BOOSTRIX®
NCT00319553 ·Status: COMPLETED ·Phase: PHASE4
-
A Study to Evaluate Long-term Safety of Ecopipam Tablets in Children, Adolescents and Adults With Tourette's Disorder
NCT06021522 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE3
-
A Study to Describe the Safety Profile and Compare the Immune Response of 4 Different Formulations of an Investigational Tdap Vaccine When Compared to Licensed Tdap Vaccine in Young Adults in Canada
NCT03958799 ·Status: COMPLETED ·Phase: PHASE1
-
Immunising Mums Against Pertussis 3
NCT03578120 ·Status: COMPLETED
-
Safety and Immunogenicity of a Booster Dose of GSK Biological's Boostrix-Polio Vaccine
NCT00635128 ·Status: COMPLETED ·Phase: PHASE4
-
COVID-19 Booster Dose Reminder/Recall for Adolescents
NCT05571657 ·Status: UNKNOWN ·Phase: NA
-
Ecopipam Tablets to Study Tourette's Syndrome in Children and Adolescents
NCT04007991 ·Status: COMPLETED ·Phase: PHASE2
-
Immunogenicity and Safety of Tetanus, Diphtheria and Mono Component Acellular Pertussis (TdaP) Vaccine in Comparison to Tetanus and Diphtheria (Td) Vaccine When Given as Booster Vaccinations to Adults
NCT01033877 ·Status: COMPLETED ·Phase: PHASE3
-
Traveler's Diarrhea (TD) Automated Process
NCT00751777 ·Status: COMPLETED ·Phase: PHASE2
-
Study of BK1301 (DTaP Vaccine) as a Booster in Adolescents
NCT02118961 ·Status: COMPLETED ·Phase: PHASE3
-
Immunogenicity and Safety of Diphtheria, Tetanus, Pertussis (DTaP) Vaccine in 3-month-old Infants
NCT06344065 ·Status: RECRUITING ·Phase: PHASE3