CClinicalTrials.gg
Status unknownNCT03024788Updated May 8, 2017

Determination of the Optimum Cut-off Value of Type 2 Diabetes Diagnosis Among Chinese Population(SENSIBLE STUDY II)

An observational study in Type II Diabetes, sponsored by Zhongda Hospital. Status unknown. Open to participants aged 20 Years to 70 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2017-05-08.

Sponsored by Zhongda Hospital · Observational

The sponsor has not verified this record recently (last verified May 2017), so the status shown — last known as Active, not recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
6,000
Ages
20 Years to 70 Years
Sex
All
01

Study summary

Study of the correlation between AGEsP and HbA1c and diabetic retinopathy prevalence: determination of cut-off value of AGEsP and HbA1c in type 2 diabetes diagnosis in China

Read the detailed description

To find the cut-off point of AGEsP and HbA1c for diagnosis of diabetes by drawing the logistic regression model between prevalence of retinopathy and AGEsP level and HbA1c level,and find the point where the prevalence of retinopathy changes most rapidly.

02

Conditions studied

  • Type II Diabetes

Keywords

  • Glycosylated haemoglobin
  • advanced glycation end products
03

In context

Diabetes Mellitus

10,925 studies on the registry are indexed under Diabetes Mellitus; 1,319 are open to participants now.

This study's enrollment of 6,000 is above the median of 233 across 2,220 observational studies indexed under Diabetes Mellitus.

Browse Diabetes Mellitus studies →

Lead sponsor

Zhongda Hospital is the lead sponsor of 101 studies on the registry; 40 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

Chinese natural population

Inclusion criteria

  • 20\~70 years old;
  • Volunteer to participate in this study and signed informed consent.

Exclusion criteria

Exclusion Criteria:

-

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
6,000 participants (actual)
Patient registry
No

Interventions

  • Devicesyringe, fundus camera etc

    Physical examination, fundus examination, blood and urine samples collection

06

What researchers measure

Primary outcomes

  1. prevalence of retinopathy

    the prevalence of retinopathy in different AGEsP and HbA1c levels

    Time frame: 3 years

Secondary outcomes

  1. incidence of retinopathy

    incidence of retinopathy in different AGEsP and HbA1c levels

    Time frame: 3 years

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 8, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03024788
Lead sponsor
Zhongda Hospital
Responsible party
Zilin Sun (director physician, Zhongda Hospital) — Principal investigator
First posted
Jan 19, 2017
Start date
Jan 2017
Primary completion
Jun 2020 (estimated)
Completion
Dec 2020
Last update
May 8, 2017

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in May 2017. You cannot join it, but the record below documents what was studied.

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