Skip to content

Combination Therapy of SGLT2 Inhibitor and intensive Physical Exercises, focusing on the Prevention of Muscle Mass Reduction in Patients with Type 2 Diabetes

Combination Therapy of SGLT2 Inhibitor and intensive Physical Exercises, focusing on the Prevention of Muscle Mass Reduction in Patients with Type 2 Diabetes - Combination of SGLT2 inhibitor and Intensive Exercise in Diabetes.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000020263
Enrollment
146
Registered
2015-12-18
Start date
2016-06-16
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 2 diabetes patients

Interventions

Five mg of dapagliflozin is to be administered orally once a day for 24 weeks, and walking of 6000 steps or more per day is practiced. Five mg of dapagliflozin is to be administered orally once a day

Sponsors

Graduate School of Medical Sciences, Kyushu University,
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Type 2 diabetic patients with age of 20 years old or older but below 75 years old 2)Patients whose BMI is 18.5 kg/m2 or higher but below 35.0 kg/m2 3)Patients whose HbA1c is 6.5% or higher but below10.0% (examination values of week 0 are to be applicable) 4)Patients whose eGFR is 45 mL/min/1.73 m2 or higher 5)Patients who have been receiving medications without any change in the administration and dosage for more than 8 weeks prior to the registration 6)Patients who can abide by the designated dietary treatment and exercise therapy 7)Patients from whom a consent in writing for the participation in this study has been obtained in person

Exclusion criteria

Exclusion criteria: 1) Type 1 diabetic patients 2) Patients with a medical history of hypersensitivity to some ingredient(s) of the SGTL2 Inhibitor 3) Patients suffering from severe ketosis, diabetic coma, or precoma 4) Patients with severe infections, patients before or after operations or having severe external injuries 5) Patients with severe renal dysfunction, or patients with end-stage renal disease or those undergoing dialysis 6) Patients with severe liver dysfunction 7) Patients who are highly likely to suffer from dehydration 8) Patients with pituitary gland dysfunction or adrenal gland dysfunction 9)Patients in dystrophia conditions, starvation status, irregular meal intake, insufficient dietary intake, or extremely weakened state 10) Patients with an excessive alcohol consumption 11) Pregnant women, patients who might be pregnant, and lactating women 12) Patients with active infectious diseases 13) Patients with malignancies 14)Patients with active diabetic proliferative retinopathy 15) Patients with glucocorticoid 16) Patients with insulin 17)Patients who have experienced hypoglycemia 3 times or more, which requires a drug treatment such as instillation with glucose before recovery 18) Patients who are judged to be inadequate to participate in this study by a doctor in charge

Design outcomes

Primary

MeasureTime frame
Change in fat free mass at 24 weeks from the base line after the administration of dapagliflozin administration with intensive exercise therapy.

Secondary

MeasureTime frame
Change in the following markers at 24 weeks from the base line after the administration of dapagliflozin administration with intensive exercise therapy. 1) HbA1c 2) Serum adiponectin 3) Leptin 4) IL-6 5) high-sensitive TNF-alpha 6) High sensitivity CRP 7) Body weight 8) Blood pressure 9) The urinary albumin-to-creatinine ratio 10) An implementation rate and degree of an exercize therapy 1,The number of steps 2,Activity time of 3.0 Mets or more 3,The number of implementation times of the resistance exercize and the number of sets.Only the groupe concomitantly performing the intensive exercize.

Countries

Japan

Contacts

Public ContactNaohide Noumi

IBEC Co.,Ltd. CEO office

research@ibec-jp.com06-7172-1751

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026