Needle Stick Clinical Trial
Official title:
Simulated Clinical Use Testing on the DropSafe Safety Pen Needle
Verified date | January 2019 |
Source | HTL-Strefa S.A. |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
A simulated clinical use testing on the DropSafe safety pen needle
Status | Completed |
Enrollment | 35 |
Est. completion date | December 9, 2016 |
Est. primary completion date | December 9, 2016 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: 1. Minimum of age 18. 2. Able to understand and provide signed consent for the study. 3. Willing to comply with the study protocol, including being willing to answer questions and complete questionnaires. 4. Have no concerns about the ability to perform the simulated injections. 5. Have no financial interest in the sponsor (HTL-Strefa S.A.) or the MRO (NAMSA). Exclusion Criteria: 1. If in the opinion of the sponsor or MRO, including the observer/monitor, the potential evaluator is not a good candidate for the study, including for reasons such as mental health. |
Country | Name | City | State |
---|---|---|---|
United States | NAMSA | Golden Valley | Minnesota |
United States | NAMSA | Minneapolis | Minnesota |
Lead Sponsor | Collaborator |
---|---|
HTL-Strefa S.A. |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The true failure rate of DropSafe safety pen needle. | The failure rate of the safety feature for the DropSafe safety pen needle was estimated using the proportion of devices that fail out of the total tested. Failure was defined as NSI or contact with the needle after injection or non-complete activation of the safety feature. | At time of testing, about an hour | |
Secondary | Ease of use | Evaluator questionnaire using five-point response scale (strongly disagree - strongly agree) | At time of testing, about an hour | |
Secondary | Ability to follow the instructions for use | Evaluator questionnaire using five-point response scale (strongly disagree - strongly agree) | At time of testing, about an hour | |
Secondary | Ease of understanding the instructions for use | Evaluator questionnaire using five-point response scale (strongly disagree - strongly agree) | At time of testing, about an hour | |
Secondary | Problems associated with the device | Evaluator questionnaire using five-point response scale (strongly disagree - strongly agree) | At time of testing, about an hour |
Status | Clinical Trial | Phase | |
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