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Effects of SGLT-2 inhibitor on appetite, food craving, and body weight

Effects of SGLT-2 inhibitor on appetite, food craving, and body weight

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0009925
Enrollment
60
Registered
2024-11-13
Start date
2017-02-22
Completion date
Unknown
Last updated
2024-11-14

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

Conditions

None listed

Interventions

Drug : Clinical trial participants will be randomly assigned to either the experimental group (SGLT-2 inhibitor group) or the active control group (DPP-4 inhibitor group) and will take dapagliflozin 1

Sponsors

The Catholic University of Korea, Seoul St. Mary's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - Type 2 diabetes patients - Age 20 years or older and 70 years or younger - Fasting blood glucose = 130 mg/dl, postprandial blood glucose = 180 mg/dl, or HbA1c = 6.5% - BMI = 20 kg/m2 - Patients with preserved renal function (eGFR = 60 ml/min/1.73 m2) - Those who agree to participate in this study

Exclusion criteria

Exclusion criteria: - Type 1 diabetes, gestational diabetes, and other secondary diabetes (e.g., diabetes after pancreatectomy, diabetes due to steroid use, etc.) - Under 20 years of age, over 70 years of age - If there has been a change in diabetes treatment medication within the past month - If SGLT-2 inhibitor or DPP-IV inhibitor has been administered within the past month - BMI <20 kg/m2 - Patients with impaired renal function (eGFR <60 ml/min/1.73 m2) - If there is a malignancy, severe infection, severe renal/liver disease, chronic pancreatitis, alcohol dependence, etc. - If there is a history of recurrent urinary tract infections - If taking medication for weight control or participating in a weight control program - If taking loop diuretics

Design outcomes

Primary

MeasureTime frame
The difference in weight loss (kg) between the experimental group and the control group at week 24 compared to baseline.

Secondary

MeasureTime frame
The proportion of participants with HbA1c <6.5% at week 24.;The changes in HbA1c, FBS, lipid profile, ketone levels, and BP from baseline to week 24.; The changes in appetite-related hormones (leptin, peptide YY, neuropeptide Y, GLP-1 total) from baseline to week 24.; The changes in dietary behavior and food craving scores from baseline to week 24.; The changes in total daily energy expenditure and carbohydrate intake from baseline to week 24.

Countries

Korea, Republic of

Contacts

Public ContactEun Young Lee

The Catholic University of Korea, Seoul St. Mary's Hospital

leyme@catholic.ac.kr+82-2-2258-6274

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026