Trials / Withdrawn
WithdrawnNCT03242005
The PSIQS Study - User Experience With Pro-Set
The PSIQS Study - User Experience With the Pro-Set Over Intended Wear of 3 Days With New Instructions and Requirement to be Inserted With the Quick-Serter
- Status
- Withdrawn
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 0 (actual)
- Sponsor
- Becton, Dickinson and Company · Industry
- Sex
- All
- Age
- 13 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
Open label, randomized 2-period cross-over study comparing two continuous subcutaneous insulin infusion sets ; MiniMed® Pro-set® with BD FlowSmart™ technology and MiniMed® Quick-set®
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | MiniMed® Pro-set® | Utilization of the MiniMed® Pro-set® to administer the subject's current insulin therapy. |
| DEVICE | MiniMed® Quick-set® | Utilization of the MiniMed® Quick-set® to administer the subject's current insulin therapy. |
Timeline
- Start date
- 2017-09-01
- Primary completion
- 2017-12-01
- Completion
- 2018-02-01
- First posted
- 2017-08-08
- Last updated
- 2017-09-14
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT03242005. Inclusion in this directory is not an endorsement.