Evaluation of Zapperclick Device for Relief From Mosquito Bites

Evaluation of a Piezoelectric Device (Zapperclick) for Relief From Mosquito Bites

Mosquito bites commonly result in redness, swelling and itching. This study will determine if a device that emits a small piezo-electrical impulse can provide relief from these symptoms. Volunteers entering the study will have a mosquito bite on one forearm. Redness and irritation will be recorded periodically for 24 hours. Comparing data from subjects randomised to the treatment or a placebo device will be analysed to determine effectiveness of the product. We will also ask the subjects their view on how easy the product is to use and clarity of instructions provided.

Study Overview

Study Type

Interventional

Enrollment (Anticipated)

120

Phase

  • Phase 3

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • London, United Kingdom, WC1E 7HT
        • London School of Hygiene & Tropical Medicine

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

16 years to 60 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • known rection to mosquito bites
  • willing to attend clinic for 2 hours during measurements
  • informed written consent

Exclusion Criteria:

  • hypersensitivity to bites or stings
  • atopic allergy
  • pacemaker
  • pregnant / breast feeding
  • use of other medication including pain killers

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: 1
Use of zapperclick on mosquito bite
Device deliveres small piezoelectrical discharge to bite site (forearm)
Placebo Comparator: 2
use of inactivated zapperclick on mosquito bite
placebo

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
reduction in itching
Time Frame: 24 hours
24 hours

Secondary Outcome Measures

Outcome Measure
Time Frame
reduction in erythema / oedema
Time Frame: 24 hours
24 hours

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

March 1, 2008

Primary Completion (Actual)

November 1, 2008

Study Completion (Anticipated)

February 1, 2009

Study Registration Dates

First Submitted

January 16, 2009

First Submitted That Met QC Criteria

January 16, 2009

First Posted (Estimate)

January 19, 2009

Study Record Updates

Last Update Posted (Estimate)

January 19, 2009

Last Update Submitted That Met QC Criteria

January 16, 2009

Last Verified

January 1, 2009

More Information

Terms related to this study

Other Study ID Numbers

  • LSHTM/HILL/08/01

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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