Prospective Study of the Impact of Insulin Pump Therapy in Young Children With Type 1 Diabetes
|
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT00727220 |
|
Recruitment Status :
Completed
First Posted : August 1, 2008
Results First Posted : May 19, 2017
Last Update Posted : May 19, 2017
|
- Study Details
- Tabular View
- Study Results
- Disclaimer
- How to Read a Study Record
| Condition or disease |
|---|
| Type 1 Diabetes |
| Study Type : | Observational |
| Actual Enrollment : | 42 participants |
| Observational Model: | Cohort |
| Time Perspective: | Prospective |
| Official Title: | A Prospective Study of the Impact of CSII Therapy in Young Children With Type 1 DM |
| Study Start Date : | November 1999 |
| Actual Primary Completion Date : | April 2003 |
| Actual Study Completion Date : | January 2004 |
| Group/Cohort |
|---|
|
Insulin Pump Therapy
Children starting insulin pump therapy
|
|
Insulin Injections
Children remaining on insulin injections.
|
- Change in HgBA1c [ Time Frame: Baseline and 6 months ]
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 1 Year to 5 Years (Child) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- Children with Type I diabetes:
- Children must be 5 years of age or less at the time of entry into the study.
- Children must have had a diagnosis of type I diabetes for at least 1 year at time of entry.
- Children must be receiving two or more insulin injections daily.
Exclusion Criteria:
- Children will be excluded if they have additional medical problems requiring treatment with agents known to affect blood glucose such as steroids or L-asparaginase.
- Children must not have any other chronic illness in addition to diabetes.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00727220
| United States, Indiana | |
| Riley Hospital for Children | |
| Indianapolis, Indiana, United States, 46202 | |
| Principal Investigator: | Linda DeMeglio, MD | Indiana University School of Medicine |
| Responsible Party: | Linda DiMeglio, MD, MD, Indiana University |
| ClinicalTrials.gov Identifier: | NCT00727220 |
| Other Study ID Numbers: |
0312-13 |
| First Posted: | August 1, 2008 Key Record Dates |
| Results First Posted: | May 19, 2017 |
| Last Update Posted: | May 19, 2017 |
| Last Verified: | May 2017 |
|
type 1 diabetes continuous glucose sensor monitoring |
|
Diabetes Mellitus, Type 1 Diabetes Mellitus Glucose Metabolism Disorders Metabolic Diseases |
Endocrine System Diseases Autoimmune Diseases Immune System Diseases |

