Navigator II Continuous Glucose Monitor Home Use Study
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| ClinicalTrials.gov Identifier: NCT01455064 |
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Recruitment Status :
Completed
First Posted : October 19, 2011
Results First Posted : July 22, 2013
Last Update Posted : July 22, 2013
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| Condition or disease | Intervention/treatment |
|---|---|
| Diabetes | Device: FreeStyle Navigator II Continuous Glucose Monitoring System |
| Study Type : | Observational |
| Actual Enrollment : | 31 participants |
| Observational Model: | Cohort |
| Time Perspective: | Prospective |
| Official Title: | FreeStyle Navigator II Continuous Glucose Monitor Home Use Evaluation (FSNv2) |
| Study Start Date : | October 2011 |
| Actual Primary Completion Date : | December 2011 |
| Actual Study Completion Date : | January 2012 |
| Group/Cohort | Intervention/treatment |
|---|---|
| Type 1 or 2 diabetes, MDI or pump |
Device: FreeStyle Navigator II Continuous Glucose Monitoring System
This is not an interventional study. Subjects must maintain their own diabetes treatment regimen throughout the study duration |
- Clarke Error Grid Analysis [ Time Frame: 15 days sensor wear ]Percentage of CGM results in the clinically accurate Zone A and percentage of CGM results in the clinically acceptable Zones A and B of the Clarke Error Grid versus blood glucose reference.
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: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
The subject must:
- Have type 1 or 2 diabetes for at least 2 years prior to enrollment.
- Require insulin therapy administered through an insulin pump or multiple daily injections (MDI) for at least 6 months prior to enrollment.
- Be at least 18 years of age.
- Be able to read and understand English.
- In the investigator's opinion, be able to follow the instructions provided to him/her by the study site and perform all study tasks as specified by the protocol.
- Be available for all study visits.
- Be willing to provide written signed and dated informed consent.
Exclusion Criteria:
The subject must not:
- Be pregnant or likely to become pregnant during the study duration.
- Have skin abnormalities at the insertion sites.
- Have known allergy to medical grade adhesive or skin disinfectant.
- Be using a continuous glucose monitor currently or within the past 6 months
- Have a concomitant medical condition which, in the opinion of the investigator, could interfere with the study or present a risk to the safety or welfare of the subject.
- Be participating in another clinical trial.
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): NCT01455064
| United States, Georgia | |
| Atlanta Diabetes Associates | |
| Atlanta, Georgia, United States, 30309 | |
| United States, New Mexico | |
| Southwest Clinical Research Center | |
| Santa Fe, New Mexico, United States, 87505 | |
| Study Director: | Shridhara A Karinka, Ph.D. | Abbott Diabetes Care |
| Responsible Party: | Abbott Diabetes Care |
| ClinicalTrials.gov Identifier: | NCT01455064 |
| Other Study ID Numbers: |
ADC11-106 |
| First Posted: | October 19, 2011 Key Record Dates |
| Results First Posted: | July 22, 2013 |
| Last Update Posted: | July 22, 2013 |
| Last Verified: | May 2013 |

