Skip to content

Study on the application value of liraglutide in patients with sepsis and hyperglycemia

Study on the application value of liraglutide in patients with sepsis and hyperglycemia

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100042480
Enrollment
Unknown
Registered
2021-01-22
Start date
2021-01-18
Completion date
Unknown
Last updated
2021-04-26

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

Conditions

sepsis with hyperglycemia

Interventions

Liraglutide group:Use liraglutide to control glucose

Sponsors

Sichuan Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Age over 18 2) Sepsis criteria: According to the diagnostic criteria of Sepsis 3.0 , for infected or suspected infection patients, SOFA = 2 points can be diagnosed as sepsis; qSOFA score is also used, that is, systolic blood pressure = 100 mmHg (1 mmHg=O 133 kPa), respiratory rate (RR) =22 beats/min, changes in consciousness, and two or more positive scores can be diagnosed as sepsis. Diagnosis was reviewed by two attending physicians referring to Sepsis 3.0 to the included patients with sepsis. At the same time, various clinical indicators were used to score SOFA and qSOFA. If there is any objection, please refer to the superior physician for judgment. 3) Patients diagnosed with stress hyperglycemia (blood sugar greater than 10mmol/L) or basic diabetes mellitus at the same time.

Exclusion criteria

Exclusion criteria: 1) Women who are pregnant or breastfeeding or plan to become pregnant during the study period. 2) Patients with type 1 diabetes. 3) Type 2 diabetes, daily insulin dose> 0.5 IU/kg. 4) Are using GLP-1 analogs and DDF-4 inhibitors for treatment, or are severely allergic to any ingredient in liraglutide; 5) History of pancreatic surgery or acute or chronic pancreatitis, personal or family history of medullary thyroid carcinoma, or type 2 multiple endocrine tumor syndrome. 6) Patients with severe kidney damage, eGFR<30ml/min. 7) Subjects who do not follow the research procedures. 8) Questions about the validity of informed consent: Subjects with a history of psychosis, mental retardation, poor motivation, drug abuse (including drugs and alcohol) or other diseases that restrict the validity of informed consent in this study. 9) The researcher thinks it is not suitable to participate in this research.

Design outcomes

Primary

MeasureTime frame
continuous glucose monitoring;

Countries

China

Contacts

Public ContactRongan Liu
35279240@qq.com15928731511

Outcome results

None listed

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