CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 64 enrolled
Drug / intervention
Canagliflozin 300 mg +2 moredrug
Likely dose
Canagliflozin 300 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03267576
NCT03267576Phase 4Completed

Canagliflozin Continuous Glucose Monitoring (CANA CGM) Trial: A Pilot Randomized, Double-Blind, Controlled, Crossover Study on the Effects of the SGLT-2 Inhibitor Canagliflozin (vs. the DPP-4 Inhibitor Sitagliptin) on Glucose Variability in Mexican Patients With Type 2 Diabetes Mellitus Inadequately Controlled on Metformin

Janssen Research & Development, LLC·interventional·Posted Aug 30, 2017·Updated Nov 29, 2019

In Brief

A Phase 4 clinical trial evaluating Canagliflozin 300 mg, Sitagliptin 100 mg, and 1 other intervention for Diabetes Mellitus, Type 2. Completed, enrolled 64 participants across 5 sites.

Detailed Summary

The main purpose of this study is to assess the effects of 4 weeks each of daily treatment with canagliflozin 300 milligram (mg) versus sitagliptin 100 mg as treatment adjuncts to metformin (at stable dosages) on intrapatient glycemic coefficient of variation (CV), expressed as a ratio percentage of standard deviation (SD) to mean glucose levels.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesMexico
Collaborators--

Timeline

Phase 4CompletedFinished
201820192020202120222023202420252026
First PostedAug 30, 2017
Enrollment StartOct 27, 2017
Primary CompletionOct 1, 2018
TodayJul 2, 2026
Enrollment to primary: 11 monthsPosted 8.8 years ago

Interventions

Canagliflozin 300 mgdrug

Participants will receive canagliflozin 300 mg oral tablet once-daily for 28 days.

Sitagliptin 100 mgdrug

Participants will receive sitagliptin 100 mg oral tablet once-daily for 28 days.

Metformindrug

Participants will receive metformin at a stable dose of \>= 1500 mg/day throughout the study including the washout period between each intervention.