Evaluating the safety and effectiveness of Sigol insect repellent spray
Phase 2
- Conditions
- Insect bite (nonvenomous).
- Registration Number
- IRCT20150101020514N21
- Lead Sponsor
- Akhavi laboratory
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 10
Inclusion Criteria
Ages 18 to 60
Signing consent form to participate in the study
Observing the study conditions and tendency to attend regular follow-up courses
Insensitivity of volunteers to the experimental herbal composition
Insensitivity or mild sensitivity to mosquito bites
Exclusion Criteria
Documented sensitivity to formulation components
susceptibility to mosquito bites
active smokers
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Estimated full protection time (Measurement of repellent application time up to the first mosquito landing or exploration ). Timepoint: A three-minute interval. Method of measurement: Using a digital camera.
- Secondary Outcome Measures
Name Time Method