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Completed

NCT Number: NCT05677334

Combination of Henagliflozin and Continuous Subcutaneous Insulin Infusion in T2DM

The Multi-center, randomized, controlled clinical trial investigate the efficacy and safety of Henagliflozin combined with continuous subcutaneous insulin infusion in newly diagnosed type 2 diabetes

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Key information

Age range

20 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

First Affiliated Hospital of Guangxi Medical University

Nanning, Guangxi, 530021, China

About this study

The therapeutic mechanisms of Sglt2i and continuous subcutaneous insulin infusion (CSII) are complementary. We hypothesized that for newly diagnosed type 2 diabetes (T2DM) with severe hyperglycemia, combination treatment with Henagliflozin and CSII could achieve glycaemic control in a shorter time, shorten the duration of hospitalization and reduce the total insulin dosage. We also hope to investigate the safety of sglt2i in combination with CSII in T2DM based on continuous glucose monitoring system.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosed as type 2 diabetes mellitus, diagnosis time ≤ 2 years
  • Age between 20 and 70 years
  • Continuous use of any hypoglycemic drug ≤ 7 days within 6 months
  • 9% ≤ HbA1c ≤ 14% or fasting blood glucose ≥ 11.1 mmol/L
  • Body mass index (BMI) of between 20 and 32 kg/m2
  • Be able to understand the contents and methods of this study and sign the informed consent form voluntarily

Exclusion criteria

  • Diabetic ketosis or ketoacidosis, diabetic hypertonic state, diabetic lactic acidosis and other acute diabetic complications or serious chronic diabetic complications
  • Urinary tract infection or/and genital infection with clinical significance, or repeated urinary tract infection or/and genital infection history
  • Serious trauma or acute infection occurred within 4 weeks that may affect blood glucose control
  • People with negligent compensatory heart failure (NYHA grade III and IV), unstable angina, stroke or transient ischemic attack, myocardial infarction, serious arrhythmia, cardiac surgery or vascular reconstruction within 6 months
  • Serious blood system disease (such as aplastic anemia, myelodysplastic syndrome) or any disease causing hemolysis or erythrocyte instability (such as malaria, hemolytic anemia)
  • Severe chronic gastrointestinal diseases, or those who have received treatment that may affect drug absorption (such as gastrointestinal surgery)
  • Uncontrolled hyperthyroidism
  • Those who have mental or nervous system diseases and are unwilling to communicate or cannot fully understand and cooperate
  • Pregnant or lactating women
  • ALT>3.0x ULN and/or AST>3.0x ULN and/or Tbil>2.0x ULN Blood ketone body>ULN eGFR<30ml/min/1.73 m2 Blood creatine kinase>3.0x ULN

Treatment and study plan

Henagliflozin

Drug

Combination therapy of Henagliflozin and Continuous Subcutaneous Insulin Infusion

Other names: Continuous Subcutaneous Insulin Infusion

Continuous Subcutaneous Insulin Infusion

Device

Continuous Subcutaneous Insulin Infusion therapy alone

Primary outcomes

  1. Time percentage (% TIR) in the range of 3.9~10.0 mmol/L blood glucose

    Time frame: Monitoring 5-14 days

    Compare the TIR of the two treatment groups

Secondary outcomes

  1. Time taken for TIR >70%

    Time frame: 5-14 days after treatment

    Compare the time required for TIR >70% of the two groups

  2. Mean Amplitude of Glycemic Excursions (MAGE)

    Time frame: 5-14 days after treatment

    Compare the mage of the two treatment groups

  3. time below range (TBR)

    Time frame: 5-14 days after treatment

    Compare the TBR of the two treatment groups

  4. total insulin dosage

    Time frame: 5-14 days after treatment

    Compare the total insulin dosage of the two treatment groups

  5. time above range (TAR)

    Time frame: 5-14 days after treatment

    Compare the TAR of the two treatment groups

Sponsors and collaborators

Lead sponsor

First Affiliated Hospital of Guangxi Medical University

Other

Registry information

Official study title

Study on the Efficacy and Safety of Henagliflozin Combined with Continuous Subcutaneous Insulin Infusion in the Treatment of Type 2 Diabetes Mellitus Based on Continuous Glucose Monitoring System

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Jan 10, 2023
Registry last updated
Mar 12, 2025

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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