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Status unknownNCT02719756Updated Mar 25, 2016

Effect of SGLT-2 Inhibitor Dapagliflozin on Glycemic Variability in Patients With Diabetes Mellitus Type 2

A Phase 4 interventional study of Metformin and Dapagliflozin in Diabetes Mellitus and Hypoglycemic Episodes, sponsored by Research Clinical Centre of the Russian Railways, JSC. Status unknown at 1 site in Russia. Open to participants aged 18 Years to 74 Years. Per ClinicalTrials.gov, last updated 2016-03-25.

Sponsored by Research Clinical Centre of the Russian Railways, JSC · Phase 4 and Interventional

The sponsor has not verified this record recently (last verified Mar 2016), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Phase 4
Study type
Interventional
Enrollment
100
Allocation
Randomized
Ages
18 Years to 74 Years
Sex
All
01

Study summary

This study will test the hypothesis that early use of combination therapy with dapagliflozin and metformin will provide good glycemic control with low glycemic variability and without hypoglycemic episodes, and will be better tolerated than up-titration of metformin monotherapy. The study will also correlate these benefits with glycated hemoglobin.

Read the detailed description

Type 2 diabetes is a progressive, chronic metabolic disease characterized by hyperglycemia. Despite therapeutic advances, the incidence and prevalence of diabetes continue to surge. Worldwide, the number of individuals with diabetes is projected to rise from 366 million in 2011 to 552 million by 2030, which is the equivalent of approximately three new cases being diagnosed every 10 seconds. Type 2 diabetes doubles the risk of cardiovascular disease, and macrovascular complications (myocardial infarction and stroke) are a common cause of death in patients with type 2 diabetes. The U.K. Prospective Diabetes Study showed that every 1% absolute decline in mean A1C was associated with a 37% reduction in the risk of microvascular complications and a 21% reduction in the risk of any diabetes-related complication or death. Diabetes also exacts a tremendous economic burden. Meeting treatment goals is elusive for many people with diabetes. Data from the National Health and Nutrition Examination Survey from 2003 to 2006 showed that only 57.1% of adults with diagnosed diabetes achieved an A1C \< 7%, 45.5% had a blood pressure level \< 130/80 mmHg, and 46.5% had an LDL cholesterol level \< 100 mg/dl. Only 12.2% of people with diabetes reached all three goals. Treatment of Type 2 diabetes is not limited to just glycaemic control. Rather, the proper management of hyperglycaemia, weight, blood pressure, and lipids can have benefits in terms of slowing the progression of Type 2 diabetes, decreasing the risk of CV disease, and improving overall health.Current antihyperglycaemic treatments are predominantly insulin-dependent. These treatments can effectively manage HbA1c, and treatment may be influenced by the patient's comorbidities and any potential treatment-related adverse events. However, as Type 2 diabetes progresses, regimens need to be modified to compensate for declining beta-cell function and decreasing insulin sensitivity. On this basis,the EASD/ADA guidelines suggest following a treatment pathway that has well validated therapies at it's core.Of the many comorbid conditions described, excess weight is especially important, not only because of the increased disease risk, but also for the management of blood pressure and lipids. Consequently, AACE/ACE algorithms give priority to those regimens that have the added benefit of minimising hypoglycaemic events and weight gain.In addition, while antidiabetic treatments tend to focus on insulin-dependent mechanisms in organs such as the liver and pancreas, it should not be forgotten that the kidneys also have a role in maintaining glucose homeostasis There are multiple barriers to achieving optimal glycemic control. Current medications for type 2 diabetes have potential adverse effects; for example, can cause hypoglycemia and weight gain. Hypoglycaemia is a limiting factor in the glycaemic management of patients with advanced Type 2 diabetes.Most often hypoglycaemia is associated with mild to severe neurologic symptoms, and in some cases it can result in death. Additionally, the risk of cardiac ischaemia is increased in Type 2 diabetes patients with symptomatic or asymptomatic hypoglycaemia compared with patients with hyperglycaemia or stable normoglycaemia. The risk of hypoglycaemia increases with advancing age, polypharmacy, later stages of disease, and intensive antihyperglycaemic treatment with certain drugs, such as sulphonylureas. Intensive treatment (target HbA1c\<7.0%) results in a greater number of patients experiencing severe hypoglycaemic events (3-21%) compared with conventional treatment (target HbA1c ≥7.0%; 2-10%), although intensive therapy may have a greater beneficial effect in terms of a decreased risk of microvascular disease. As a result, hypoglycaemia is one of several factors, including weight gain and increases in CV disease-related and overall mortality, that may limit the microvascular benefits of intensive therapy. Thus, the search continues for novel therapeutic agents that can help patients avoid these limiting side effects while providing glycemic control.

02

Conditions studied

  • Diabetes Mellitus
  • Hypoglycemic Episodes

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03

In context

Diabetes Mellitus

11,089 studies on the registry are indexed under Diabetes Mellitus; 1,319 are open to participants now.

This study's planned enrollment of 100 is above the median of 80 across 8,491 interventional studies indexed under Diabetes Mellitus.

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Lead sponsor

Research Clinical Centre of the Russian Railways, JSC is the lead sponsor of 2 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 74 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

The subject population that will be observed in the study, must fulfil all of the following criteria:

  1. Signed informed consent.
  2. Written informed consent by women of childbearing age to interception during study participation period, with determination of level of chorionic gonadotropic hormone by the pregnancy test, prior to study enrollment.
  3. Age >=18 - 74 years.
  4. eGFR >=60 mL/min/1.73 m2 by MDRD formula.
  5. BMI \<40 kg / m2
  6. C-peptide >= 1 ng/ml
  7. HbA1c 7 - 9% both included
  8. Stabile 1000 mg dose of Metformin daily for at least 8 weeks prior to enrollment

Exclusion criteria

Exclusion criteria

  1. The presence of absolute contraindications to therapy by SGLT-2 inhibitor Dapagliflozin:

    1.1. Individual idiosyncrasy of any drug component.

    1.2. Type 1 diabetes.

    1.3. Diabetic ketoacidosis.

    1.4. Renal disease, medium to severe (eGFR \<60 ml/min /1.73m2 by MDRD formula) or end-stage renal failure.

    1.5.Hereditary lactose intolerance, lactase deficiency, and glucose and galactose intolerance.

    1.6. Pregnancy and breast-feeding.

    1.7. Children under 18 years of age.

    1.8. Patients receiving loop diuretics or with reduced volume of blood circulation, such as a result of acute diseases (e.g. gastrointestinal problems).

    1.9. Elderly patients aged 75 years and older.

  2. A history of moderate or severe congestive heart failure (New York Heart Association [NYHA] Class III or IV) within 3 months prior to the screening visit
  3. Increased liver transaminases ALT and/or AST more than 3 times higher than normal.
  4. Any condition that in the opinion of the PI confound the evaluation and interpretation of efficacy and or safety data. Significant medical or psychological condition that, in the opinion of the Investigator, would compromise the patient's safety or successful participation in the study.
05

Study design

Phase
Phase 4
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
100 participants (estimated)

Study arms

  • Experimental
    Metformin & Dapagliflozin

    Metformin stable dose tablets and Dapagliflozin 10 mg tablets by mouths, once daily in morning for 3 months

    Drug: Metformin · Drug: Dapagliflozin

  • Active comparator
    Metformin up-titration

    Metformin tablets up-titration by mouths, for 3 months

    Drug: Metformin · Drug: Metformin up-titration

Interventions

  • Metformin tablets 1000 mg

    Also known as: GLUCOPHAGE

  • Dapagliflozin 10 mg tablets

    Also known as: FORXIGA, FARXIGA

  • DrugMetformin up-titration
06

What researchers measure

Primary outcomes

  1. Dynamics (delta from the baseline) of blood glucose variability - integral index of glycemia (LBGI-HBGI) after 3 months of therapy

    Time frame: 3 months

Secondary outcomes

  1. Dynamics (delta from the baseline or % decrease of blood glucose level) of blood glucose variability (ADRR) after 3 months of therapy

    Time frame: 3 months

  2. Dynamics of MAGE after 3 months of therapy

    Time frame: 3 months

  3. Dynamic of glycaemia parameters: % of normoglycemia time after 3 months of therapy

    Time frame: 3 months

  4. Dynamic of glycaemia parameters: % of hyperglycemia time after 3 months of therapy

    Time frame: 3 months

  5. Dynamic of glycaemia parameters: % of hypoglycemia time after 3 months of therapy

    Time frame: 3 months

  6. Dynamics of HbA1c (%) from baseline after 3 months of therapy

    Time frame: 3 months

  7. Percentage of diabetes mellitus patients achieved individual target HbA1c

    Time frame: 3 months

07

Study locations

1 site
  • Research Clinical Centre of the Russian Railways, JSC
    Moscow, 125993, Russia
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 25, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02719756
Lead sponsor
Research Clinical Centre of the Russian Railways, JSC
Responsible party
Sponsor
First posted
Mar 25, 2016
Start date
Apr 2016
Primary completion
Oct 2016 (estimated)
Completion
Dec 2016 (estimated)
Last update
Mar 25, 2016

Study contacts

Alexander Ametov, prof., MD
Contact
alexander.ametov@gmail.com
(499)1510951 ext. 8107
Viktoria Blagova, PhD cand.
Contact
vika-blagova@mail.ru
(499)6130363 ext. 8107
Alexander Ametov, prof., MD
principal investigator · Research Clinical Center of the Russian Railways, JSC

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

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