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Novofine Autocover Safety Needle Versus BD Safety Glide
This study has been completed.
First Received: July 13, 2005   Last Updated: October 2, 2009   History of Changes
Sponsor: Novo Nordisk
Information provided by: Novo Nordisk
ClinicalTrials.gov Identifier: NCT00121355
  Purpose

This study will examine whether nurses prefer to use the NovoFine® Autocover Needle or the BD Safety Glide (TM) Syringe (only) in a hospital setting. The number of needle stick injuries will also be evaluated and whether these hospital nurses prefer the safety features of the NovoFine® Autocover Needle versus those of the BD Safety Glide (TM) Syringe. The identified hospital nurses will evaluate the two types of needles during standard administration of insulin to patients being treated for diabetes.


Condition Intervention Phase
Health Personnel
Device: safety glide
Device: autocover needle
Phase IV

Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Uncontrolled, Crossover Assignment, Safety Study

Further study details as provided by Novo Nordisk:

Enrollment: 83
Study Start Date: July 2005
Study Completion Date: June 2006
Primary Completion Date: June 2006 (Final data collection date for primary outcome measure)
  Eligibility

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Hospital nurses with prior injection training without an infectious blood borne disease
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00121355

Locations
United States, Florida
Novo Nordisk Clinical Trial Call Center
Miami, Florida, United States, 33176
United States, Georgia
Novo Nordisk Clinical Trial Call Center
Atlanta, Georgia, United States, 30339
United States, Louisiana
Novo Nordisk Clinical Trial Call Center
New Orleans, Louisiana, United States, 70121
United States, Ohio
Novo Nordisk Clinical Trial Call Center
Cleveland, Ohio, United States, 44195
Novo Nordisk Clinical Trial Call Center
Portsmouth, Ohio, United States, 45662
Novo Nordisk Clinical Trial Call Center
Zanesville, Ohio, United States, 43701
Novo Nordisk Clinical Trial Call Center
Westerville, Ohio, United States, 43081
United States, Texas
Novo Nordisk Clinical Trial Call Center
Irving, Texas, United States, 75061
Novo Nordisk Clinical Trial Call Center
Houston, Texas, United States, 77030
Sponsors and Collaborators
Novo Nordisk
Investigators
Study Director: Campbell Howard, MD Novo Nordisk
  More Information

Additional Information:
No publications provided

Responsible Party: Novo Nordisk A/S ( Public Access to Clinical Trials )
Study ID Numbers: MS241-1674
Study First Received: July 13, 2005
Last Updated: October 2, 2009
ClinicalTrials.gov Identifier: NCT00121355     History of Changes
Health Authority: United States: Institutional Review Board

Keywords provided by Novo Nordisk:
Needles

ClinicalTrials.gov processed this record on February 08, 2010