Neuss, Germany
NCT Number: NCT01273558
A Study of Two Methods for Determining the Renal Threshold for Glucose in Patients With Type 2 Diabetes Mellitus
The purpose of this study is to compare the results from two methods used to determine the renal threshold for glucose excretion (defined as the lowest plasma glucose concentration at which appreciable amounts of glucose appear in the urine) in untreated patients with type 2 diabetes mellitus and in patients with type 2 diabetes mellitus who are treated with 100 mg once-daily canigliflozin for 8 days.
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Notify MeKey information
Conditions
Age range
18 year–65 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 1
Primary location
About this study
This is an open-label (patients will know if they are receiving treatment and the identity of the treatment) study that will compare renal threshold of glucose (RTG) values obtained by 2 different methods: an established method (ie, the stepwise hyperglycemic clamp method) and a new method (the mixed meal tolerance test [MMTT] method). The RTG is defined as the lowest plasma glucose concentration at which appreciable amounts of glucose appear in the urine. Each method for determining the RTG value will be performed in untreated patients with type 2 diabetes mellitus (T2DM) and in patients with T2DM who are treated with canagliflozin 100 mg once daily for 8 days. Canagliflozin (a Sodium-Glucose Cotransporter 2 inhibitor) is currently under development to lower blood sugar levels in patients with T2DM. Patients will not take study drug (canagliflozin 100 mg overencapsulated tablets) in Part 1 of the study. In Part 2 of the study, patients will take study drug once daily on Study Days 1 through 8.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Patients with T2DM who are not receiving treatment with any anti-hyperglycemic agents (AHAs) for at least 12 weeks, or who are receiving treatment with a stable dose and regimen of metformin monotherapy for at least 12 weeks and have a hemoglobin A1c (HbA1c) in the range of >=7% to <=10%
Exclusion criteria
- History of Type 1, "brittle" diabetes or secondary forms of diabetes
- History of 1 or more severe hypoglycemic episodes
- History of diabetic complications considered to be clinically significant by the Investigator
- History of or current illness considered to be clinically significant by the investigator
Treatment and study plan
Canagliflozin
DrugOne 100 mg capsule taken orally (by mouth) on Days Days 1-8
Primary outcomes
-
RTG values using the MMTT and the stepwise hyperglycemic clamp methods
Time frame: On Days 1 and 2 (Part 1)
-
RTG values using the MMTT and the stepwise hyperglycemic clamp methods
Time frame: On Days 7 and 8 (Part 2)
Secondary outcomes
-
Plasma glucose (PG) concentration during the MMT and the hyperglycemic clamp procedure
Time frame: On Days 1 and 2 (Part 1)
-
Plasma glucose (PG) concentration during the MMT and the hyperglycemic clamp procedure
Time frame: On Days 7 and 8 (Part 2)
-
Rate of Urinary glucose excretion (UGE) during the MMTT and the hyperglycemic clamp procedure
Time frame: On Days 1 and 2 (Part 1)
-
Rate of Urinary glucose excretion (UGE) during the MMTT and the hyperglycemic clamp procedure
Time frame: On Days 7 and 8 (Part 2)
Sponsors and collaborators
Lead sponsor
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
Industry
Registry information
Official study title
An Open-Label Study to Compare Two Methods for Determining the Renal Threshold for Glucose in Subjects With Type 2 Diabetes Mellitus
Important dates
- Study start
- 2011
- Study completion
- 2011
- First posted
- Jan 10, 2011
- Registry last updated
- Apr 22, 2013
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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