Clinical Trials Directory

Trials / Completed

CompletedNCT04253431

The Characteristics of Different Personal Lancets on Blood Volume and Perceived Pain in Patients With Diabetes Mellitus

A Single-blind, Randomized, Single-centre Study to Investigate the Characteristics of Different Personal Lancets on Blood Volume and Perceived Pain in Patients With Diabetes Mellitus

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
HTL-Strefa S.A. · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

A randomized single-blind study with the use of different lancing devices equipped with personal lancets to determine and to compare the amount of capillary blood volume and perceived pain after a single lancing of the fingertip.

Conditions

Interventions

TypeNameDescription
DEVICEDroplet lancing device (HTL-Strefa S.A.)
DEVICEMicrolet 2 lancing device (Bayer)
DEVICEOneTouch Delicia lancing device (LifeScan)
DEVICEReliOn lancing device (ReliOn)
DEVICEAccu-Chek Softclix lancing device (Roche)
DEVICEBGStar lancing device (Sanofi Aventis)
DEVICEUltra-Fine 33G lancets (BD)
DEVICEDroplet 33G lancets (HTL-Strefa S.A.)
DEVICEOneTouch Delicia Extra Fine 33G lancets (LifeScan)
DEVICEHaemoFine 33G lancets (HTL-Strefa S.A.)
DEVICESoftclix 28 G lancets (Roche)
DEVICEReliOn Ultra-Thin Plus 33G lancets (ReliOn)
DEVICEGlucoJect Dual S lancing device (Menarini)
DEVICEMicrolet 28G lancets (Bayer)
DEVICEBGStar Ultra-Thin 33G lancets (Sanofi Aventis)

Timeline

Start date
2013-08-01
Primary completion
2013-08-01
Completion
2013-08-01
First posted
2020-02-05
Last updated
2020-02-05

Source: ClinicalTrials.gov record NCT04253431. Inclusion in this directory is not an endorsement.