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

NCT04253431 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2020-02-05

No results posted yet for this study

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

  • Diabetes Mellitus, Type 1
  • Diabetes Mellitus, Type 2

Interventions

DEVICE

Droplet lancing device (HTL-Strefa S.A.)

DEVICE

Microlet 2 lancing device (Bayer)

DEVICE

OneTouch Delicia lancing device (LifeScan)

DEVICE

ReliOn lancing device (ReliOn)

DEVICE

Accu-Chek Softclix lancing device (Roche)

DEVICE

BGStar lancing device (Sanofi Aventis)

DEVICE

Ultra-Fine 33G lancets (BD)

DEVICE

Droplet 33G lancets (HTL-Strefa S.A.)

DEVICE

OneTouch Delicia Extra Fine 33G lancets (LifeScan)

DEVICE

HaemoFine 33G lancets (HTL-Strefa S.A.)

DEVICE

Softclix 28 G lancets (Roche)

DEVICE

ReliOn Ultra-Thin Plus 33G lancets (ReliOn)

DEVICE

GlucoJect Dual S lancing device (Menarini)

DEVICE

Microlet 28G lancets (Bayer)

DEVICE

BGStar Ultra-Thin 33G lancets (Sanofi Aventis)

Sponsors & Collaborators

  • HTL-Strefa S.A.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-08-31
Primary Completion
2013-08-31
Completion
2013-08-31

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04253431 on ClinicalTrials.gov