- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00567775
Comparison of Human Insulin to Insulin Inhalation Solution in Children With Type 1 Diabetes
February 28, 2017 updated by: Novo Nordisk A/S
Comparison of Pharmacokinetic Profiles of Human Soluble Insulin With Insulin Inhalation Solution in Paediatric Type 1 Diabetes Mellitus
This trial is conducted in Europe.
The aim of this trial is to compare the pharmacokinetic profile of two different methods of insulin administration in children with type 1 diabetes.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
27
Phase
- Phase 2
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Glostrup, Denmark, 2600
- Novo Nordisk Investigational Site
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
6 years to 17 years (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Type 1 diabetes
- Treatment for at least 12 months
- HbA1c lesser or equal to 11.0%
- Body weight between 25 and 80 Kg
- Capable to use the device
Exclusion Criteria:
- Any diseases other than diabetes requiring prescriptive medication
- Known or suspected allergy to trial product or related products
- Active proliferative retinopathy as judged by the Investigator
- Recurrent severe hypoglycaemia as judged by the Investigator
- The receipt of any investigational drug within 4 weeks prior to this trial
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Area under the serum insulin curve
Time Frame: from 0 to 5 hours post-dosing
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from 0 to 5 hours post-dosing
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Maximum serum insulin concentration
Time Frame: in the interval from 0 to 5 hours post-dosing
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in the interval from 0 to 5 hours post-dosing
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Time to maximum serum insulin concentration
Time Frame: in the interval from 0 to 5 hours post-dosing
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in the interval from 0 to 5 hours post-dosing
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 21, 2002
Primary Completion (Actual)
November 20, 2002
Study Completion (Actual)
November 20, 2002
Study Registration Dates
First Submitted
November 30, 2007
First Submitted That Met QC Criteria
December 4, 2007
First Posted (Estimate)
December 5, 2007
Study Record Updates
Last Update Posted (Actual)
March 1, 2017
Last Update Submitted That Met QC Criteria
February 28, 2017
Last Verified
February 1, 2017
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- NN1998-1274
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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