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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04099745
Other study ID # KY20190823-02
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date October 1, 2019
Est. completion date February 1, 2020

Study information

Verified date September 2019
Source Nanjing First Hospital, Nanjing Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To compare the accuracy of different blood glucose monitoring systems (CGM and FGM) in diabetic patients with insufficient islet function.


Description:

To compare the accuracy of different blood glucose monitoring systems (CGM and FGM) in diabetic patients with insufficient islet function with Venous Blood Glucose (including FGM early, middle and late, pre-and post-meal, high and low blood glucose).


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 30
Est. completion date February 1, 2020
Est. primary completion date December 30, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- volunteer to participate and be able to sign informed consent prior to the trial.

- patients with type 2 diabetes or type 1 diabetes, aged 18-80 years old.

- No acute complications such as diabetic ketoacidosis, diabetic hyperosmolar syndrome, etc.

- Subjects are able and willing to monitor peripheral blood sugar and regularity of diet and exercise.

Exclusion Criteria:

- Patients with insulin allergy.

- Impaired liver and kidney function with ALT 2.5 times higher than the upper limit of normal value; Serum creatinine was 1.3 times higher than the upper limit of normal.

- Drug abuse and alcohol dependence in the past 5 years.

- Systemic hormone therapy was used in the last three months.

- Patients with poor compliance and irregular diet and exercise.

- Patients with pregnancy, lactation or pregnancy intention.

- Any other obvious conditions or associated diseases determined by the researcher: such as severe cardiopulmonary diseases, endocrine diseases, neurological diseases, tumors and other diseases, other pancreatic diseases, history of mental diseases.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
CGM
Continuous Glucose Monitoring System
FGM
Flash glucose monitoring System

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Nanjing First Hospital, Nanjing Medical University

Outcome

Type Measure Description Time frame Safety issue
Primary Accuracy of different blood glucose monitoring systems (CGM and FGM) with intravenous blood glucose level as the gold standard To compare the accuracy of different blood glucose monitoring systems (CGM and FGM) with intravenous blood glucose level as the gold standard in diabetic patients with insufficient islet function. 2 weeks
Secondary three-day blood glucose fluctuation of CGM 3 DAYS
Secondary forty-day blood glucose fluctuation of FGM 14 days
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