Pilot Safety Study to Determine the Ability of the Protector Cap Jet Injector to Prevent Cross-Contamination
NCT ID: NCT00219453
Last Updated: 2007-04-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE1
17 participants
INTERVENTIONAL
2004-10-31
2006-01-31
Brief Summary
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Detailed Description
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The objective of this pilot safety study is to provide a preliminary indication of the ability of the jet injector to prevent cross-contamination from hepatitis B virus between volunteer injections. A secondary objective of the study is to test study procedures prior to a larger-scale safety study.
Conditions
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Study Design
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NON_RANDOMIZED
SINGLE_GROUP
PREVENTION
NONE
Interventions
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Jet Injector with Protector Cap (HSI-500)
Eligibility Criteria
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Inclusion Criteria
* Either male or female.
* In good health, by self-report and confirmed by physical exam.
* Willing and able to follow procedural requirements of the study.
* Willing and able to provide informed consent for study participation.
* Ability to read and understand informed consent information sheet in English.
For Hepatitis B Positive Volunteers
* Actively infected with blood levels of greater than or equal to 10\*6 hepatits B virus (HBV) copies/mL, confirmed by HBV DNA blood test conducted up to 21 days prior to the day of study enrollment (existing patient record)
* Not presently taking any heparin-based drugs that could potentially interfere with HBV assays.
For Hepatitis B Negative Volunteers
* Not actively infected with HBV as confirmed by HBV tests.
* Not presently taking any drugs that could potentially interfere with HBV assays.
* No prior history of HBV infection.
Exclusion Criteria
* History of allergic reactions or anaphylaxis to immunizations.
* Dermatological conditions affecting the injection site (such as eczema).
* Blood coagulation disorders or history of taking drugs that affect blood coagulation.
* Presently taking any heparin-based medication (Calciparine, Liquaemin Sodium, Hep-Lock, or Hep-Lock U/P) that could potentially interfere with HBV assays.
* History of severe psychiatric disease.
* Previous suicidal attempt or hospitalization for psychiatric episode within the last 24 weeks.
* Any other conditions or circumstances that, in the opinion of the investigator, may be a threat to the safety and welfare of the volunteer.
18 Years
60 Years
ALL
Yes
Sponsors
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Bill and Melinda Gates Foundation
OTHER
PATH
OTHER
Principal Investigators
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Darin L Zehrung, BS
Role: STUDY_DIRECTOR
PATH
Related Links
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August 9, 2005 FDA Safety Panel meeting information: agenda, meeting transcript, questions, and other supporting documentation.
Other Identifiers
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HS243
Identifier Type: -
Identifier Source: org_study_id