Evaluation of Zapperclick Device for Relief From Mosquito Bites
The recruitment status of this study is unknown because the information has not been verified recently.
Verified January 2009 by London School of Hygiene and Tropical Medicine.
Recruitment status was Active, not recruiting
Recruitment status was Active, not recruiting
Sponsor:
London School of Hygiene and Tropical Medicine
Information provided by:
London School of Hygiene and Tropical Medicine
ClinicalTrials.gov Identifier:
NCT00825214
First received: January 16, 2009
Last updated: NA
Last verified: January 2009
History: No changes posted
| Tracking Information | |
|---|---|
| First Received Date ICMJE | January 16, 2009 |
| Last Updated Date | January 16, 2009 |
| Start Date ICMJE | March 2008 |
| Primary Completion Date | November 2008 (final data collection date for primary outcome measure) |
| Current Primary Outcome Measures ICMJE |
reduction in itching [ Time Frame: 24 hours ] [ Designated as safety issue: No ] |
| Original Primary Outcome Measures ICMJE | Same as current |
| Change History | No Changes Posted |
| Current Secondary Outcome Measures ICMJE |
reduction in erythema / oedema [ Time Frame: 24 hours ] [ Designated as safety issue: No ] |
| Original Secondary Outcome Measures ICMJE | Same as current |
| Current Other Outcome Measures ICMJE | Not Provided |
| Original Other Outcome Measures ICMJE | Not Provided |
| Descriptive Information | |
| Brief Title ICMJE | Evaluation of Zapperclick Device for Relief From Mosquito Bites |
| Official Title ICMJE | Evaluation of a Piezoelectric Device (Zapperclick) for Relief From Mosquito Bites |
| Brief Summary | 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. |
| Detailed Description | Not Provided |
| Study Type ICMJE | Interventional |
| Study Phase | Phase 3 |
| Study Design ICMJE | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Investigator, Outcomes Assessor) Primary Purpose: Treatment |
| Condition ICMJE |
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| Intervention ICMJE |
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| Study Arm (s) |
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| Publications * | Not Provided |
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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| Recruitment Information | |
| Recruitment Status ICMJE | Active, not recruiting |
| Estimated Enrollment ICMJE | 120 |
| Estimated Completion Date | February 2009 |
| Primary Completion Date | November 2008 (final data collection date for primary outcome measure) |
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both |
| Ages | 16 Years to 60 Years |
| Accepts Healthy Volunteers | Yes |
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects |
| Location Countries ICMJE | United Kingdom |
| Administrative Information | |
| NCT Number ICMJE | NCT00825214 |
| Other Study ID Numbers ICMJE | LSHTM/HILL/08/01 |
| Has Data Monitoring Committee | No |
| Responsible Party | Dr. Nigel Hill, Head of Unit, DCVBU. Principle Investigator, LSHTM |
| Study Sponsor ICMJE | London School of Hygiene and Tropical Medicine |
| Collaborators ICMJE | Not Provided |
| Investigators ICMJE | Not Provided |
| Information Provided By | London School of Hygiene and Tropical Medicine |
| Verification Date | January 2009 |
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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