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Evaluation of Innovated Screening Tools for Type 2 Diabetes Among Chinese Population(SENSIBLE STUDY I)

Using 2h-glycosuria Combined With Fasting Plasma Glucose , Advanced Glycation End-product Alone or in Combination With Fasting Plasma Glucose in Diabetes Screening in Chinese Natural Population

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03025919
Enrollment
20000
Registered
2017-01-20
Start date
2017-01-31
Completion date
2017-12-31
Last updated
2017-05-08

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

Conditions

Type II Diabetes Mellitus

Keywords

Advanced glycation end-product, Glycosuria

Brief summary

Evaluation of using 2h-UG combined with FPG, AGEsP alone or in combination with FPG in diabetes screening in Chinese natural population

Detailed description

Using the WHO criteria as the golden standard,drawing the ROC curve of 2h-UG combined with FPG, AGEsP alone or in combination with FPG,calculating the area under the ROC curve.

Interventions

None listed

Sponsors

Zhongda Hospital
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
12 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* 20\ 70 year old urban and rural residents; * Volunteer to participate in this study and sign informed consent.

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
area under the ROC curve6 monthsarea under the ROC curve of different method of using 2h-UG combined with FPG, AGEsP alone or in combination with FPG in diabetes screening in Chinese natural population

Secondary

MeasureTime frameDescription
sensitivity and specificity of screening6 monthsUsing WHO criteria as golden standard,sensitivity and specificity of using 2h-UG combined with FPG, AGEsP alone or in combination with FPG in diabetes screening in Chinese natural population

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026