Fact CheckerSign in

NCT07711171RecruitingPhase 4

Efficacy and Safety of Canagliflozin in the Treatment of Type 2 Diabetes With Mild Cognitive Impairment

Efficacy and Safety of Canagliflozin in the Treatment of Type 2 Diabetes With Mild Cognitive Impairment- a Prospective, Randomized, Single-blind, Controlled, Single-center, Head-to-head Clinical Cohort Study

Source: ClinicalTrials.gov · Last updated 17 Jul 2026

Brief summary (registry, in English)

The prevalence of cognitive dysfunction in diabetic patients is high, which seriously affects the quality of life of patients, and early intervention is of great significance. Central nervous system insulin resistance plays a key role in the pathogenesis of cognitive dysfunction in diabetic patients. Central insulin resistance observed by functional magnetic resonance imaging (fMRI), may serve as an alternative endpoint for assessing cognitive function. Sodium glucose cotransporter 2 inhibitor (SGLT2i) may improve cognitive impairment by improving central insulin resistance.

Status (registry)
Recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
60 (estimated)
First submitted
2 Feb 2024
Start date
19 Aug 2024
Primary completion date
30 Oct 2026
Lead sponsor
Fudan University
NCT number
NCT07711171

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 60
  • From 19 Aug 2024 to the primary completion date, 30 Oct 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • alcohol or drug addiction history;
  • use of other oral hypoglycemic drugs within 90 days prior to enrollment except for metformin;

Other illness

  • duration of diabetes is less than 6 years;
  • Family or past history of neurological or psychiatric disorders, pancreatitis, medullary thyroid cancer and multiple endocrine adenomatosis;
  • History of recurrent urinary tract infection and malignant tumor;
  • History of severe gastrointestinal diseases and gastroenteric surgery;
  • Abnormal liver function (liver enzyme index is more than 2.5 times the upper limit of the reference range) or abnormal kidney function (estimated glomerular filtration rate is less than 45ml/min); Type 1 diabetes; other diseases or conditions that reduce the possibility of enrollment or complicate enrollment, such as frequent changes in the working environment and unstable living environment, which are likely to cause loss of follow-up, according to the judgment of the researchers;

Other

  • left-handedness;
  • inability to complete central nervous system magnetic resonance imaging;
  • Pregnancy/lactation status;

Who the study is looking for

  • age: 40-75 years old;
  • HbA1c: 7.0 - 10.0%;
  • Moca scale total score between 20-26 (duration of education is more than 10 years) or total score between 20 and 25 (duration of education is less than 10 years);
  • sign informed consent;

Age in the registry: 40 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Fudan University Affiliated Huadong Hospital
Coordinator of this site? Confirm its status
ShanghaiChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.