Trials / Completed
CompletedNCT03479619
Comparison of Three Lancing Devices Regarding Capillary Blood Volume and Lancing Pain Intensity.
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 90 (actual)
- Sponsor
- HTL-Strefa S.A. · Industry
- Sex
- All
- Age
- 18 Years – 50 Years
- Healthy volunteers
- Not accepted
Summary
A randomized single-blind study with the use of three lancing devices equipped with personal lancets. Every device will be studied for three lancet sizes: 28G, 30G, and 33G with the minimum and maximum puncture depth setting.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Lancing device A | Glucoject Dual Plus lancing device |
| DEVICE | Lancing device B | Droplet lancing device |
| DEVICE | Lancing device C | Commercially available lancing device |
| DEVICE | 28 G lancet | Droplet 28 G |
| DEVICE | 30 G lancet | Droplet personal lancet 30 G |
| DEVICE | 33 G lancet | Droplet personal lancet 33 G |
| OTHER | Lancing depth setting (1) | The lowest depth setting (1) |
| OTHER | Lancing depth setting (5) | The highest depth setting (5) |
Timeline
- Start date
- 2018-03-06
- Primary completion
- 2018-05-14
- Completion
- 2018-09-27
- First posted
- 2018-03-27
- Last updated
- 2020-02-05
Locations
1 site across 1 country: Poland
Source: ClinicalTrials.gov record NCT03479619. Inclusion in this directory is not an endorsement.