ClinicalTrials.gov
 Home    Search    Study Topics    Glossary  
 

  Full Text View  
  Tabular View  
  Contacts and Locations  
  No Study Results Posted  
  Related Studies  
Hospital In-Patient Insulin Study

This study has been terminated.
( No documentation with MHRA to support clinical trial of a medicinal product. )

Sponsored by: The Royal Bournemouth Hospital
Information provided by: The Royal Bournemouth Hospital
ClinicalTrials.gov Identifier: NCT00135070
  Purpose

Hyperglycaemia has been shown to increase morbidity and mortality in patients with critical illness, myocardial infarction and stroke. This study aims to look at patients with hyperglycaemia and reduce their blood sugar levels using differing combinations of subcutaneous and intravenous insulin.


Condition Intervention Phase
Diabetes Mellitus, Type 2
Drug: Detemir
Phase IV

MedlinePlus related topics:   Diabetes   

ChemIDplus related topics:   Insulin   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Safety/Efficacy Study
Official Title:   A Randomised Study Comparing Continuous Intravenous Insulin Infusion With Subcutaneous Insulin Analogues in Hospitalised Patients With Type II Diabetes and Hyperglycaemia

Further study details as provided by The Royal Bournemouth Hospital:

Primary Outcome Measures:
  • Glucose control

Secondary Outcome Measures:
  • Length of stay

Enrollment:   41
Study Start Date:   July 2005
Study Completion Date:   June 2006

Detailed Description:

This is a randomised trial involving patients with type II diabetes who are brought into the hospital with a problem other than a diabetic emergency. Patients will be included, who have a blood sugar > than 17mmols. They will be randomised to one of two groups and either given intravenous or subcutaneous insulin. Outcome measures are length of stay, glucose control and comparison of the two regimens. Cost implications will also be analysed.

  Eligibility
Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

Inclusion Criteria:

  • Type II diabetes
  • Blood glucose > 17mmols

Exclusion Criteria:

  • Type I diabetes
  • Hyperosmolar non-ketotic coma (HONK)
  • Diabetic ketoacidosis (DKA)
  • Myocardial infarction (MI)
  • Vomiting
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00135070

Locations
United Kingdom, Dorset
The Royal Bournemouth Hospital    
      Bournemouth, Dorset, United Kingdom, BH7 7DW

Sponsors and Collaborators
The Royal Bournemouth Hospital

Investigators
Principal Investigator:     David Kerr, Doctor     The Royal Bournemouth Hospital    
  More Information


Study ID Numbers:   H.P.I.1
First Received:   August 23, 2005
Last Updated:   April 27, 2007
ClinicalTrials.gov Identifier:   NCT00135070
Health Authority:   United Kingdom: Research Ethics Committee

Keywords provided by The Royal Bournemouth Hospital:
Diabetes Mellitus  

Study placed in the following topic categories:
Metabolic Diseases
Hyperglycemia
Diabetes Mellitus, Type 2
Diabetes Mellitus
Endocrine System Diseases
Endocrinopathy
Metabolic disorder
Glucose Metabolism Disorders
Insulin

ClinicalTrials.gov processed this record on October 17, 2008




Links to all studies - primarily for crawlers