Shanghai Cohort Study of Diabetic Eye Disease (SCODE)
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| ClinicalTrials.gov Identifier: NCT03665090 |
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Recruitment Status : Unknown
Verified September 2018 by Jiannan Huang, Shanghai Eye Disease Prevention and Treatment Center.
Recruitment status was: Enrolling by invitation
First Posted : September 11, 2018
Last Update Posted : September 11, 2018
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| Condition or disease | Intervention/treatment |
|---|---|
| Diabetic Macular Edema of Both Eyes (Diagnosis) Diabetic Retinopathy Visually Threatening | Behavioral: Diabetic eye disease screening |
The Shanghai Cohort study of Diabetic Eye disease (SCODE) was a three-year community-based study to carry out a regular ocular health screening and epidemiological analysis for diabetic eye disease in the approximately 8,000 middle-aged and elderly people with diabetes in Shanghai. Through this study, we hope to understand the prevalence, epidemic trend and the features of risk factors distribution on diabetic eye disease, especially on DR.
Meanwhile, our aims also included estimating the ocular fundus changes and visual impairment associated with different grade of DR. Furthermore, the aim of the present study was to investigate the association between serum and urine biochemical parameters and DR.
| Study Type : | Observational |
| Actual Enrollment : | 8000 participants |
| Observational Model: | Cohort |
| Time Perspective: | Prospective |
| Official Title: | A Three-year Community-based Study in Diabetes: The Shanghai Cohort Study of Diabetic Eye Disease |
| Actual Study Start Date : | January 1, 2016 |
| Estimated Primary Completion Date : | December 31, 2018 |
| Estimated Study Completion Date : | December 31, 2020 |
- Behavioral: Diabetic eye disease screening
Community-based, prospective cohort study from three consecutive years (2016 to 2018) to determine the prevalence and impact of diabetic eye disease, especially diabetic retinopathy (DR), in adults with diabetes living in Shanghai.
- Prevalence and incidence rate of diabetic eye disease [ Time Frame: December 31, 2018 ]SCODE was performed to evaluate the prevalence and rate of new cases of diabetic eye disease, especially DR, in a three-year community-based cohort study for the people with diabetes, and to identify the associated factors related with diabetic eye disease.
- Grading of DR [ Time Frame: December 31, 2018 ]Fundus changes were evaluated on non-mydriatic fundus photography and slit-lamp examination. Meanwhile, we will estimate the fundus changes associated with different grade of DR.
- Retinal and choroidal thickness [ Time Frame: December 31, 2018 ]Retinal and choroidal thickness were evaluated on SS-OCT.
- Retinal blood flow [ Time Frame: December 31, 2018 ]Retinal blood flow were evaluated on SD-OCTA.
- Blood biochemistry indexes [ Time Frame: December 31, 2018 ]Blood samples were used for testing, including glucose, glycosylated hemoglobin (HbA1C), serum lipids, etc.
- Urine biochemistry indexes [ Time Frame: December 31, 2018 ]Urine samples were used for testing urine albumin and creatinine.
- Visual impairment [ Time Frame: December 31, 2018 ]Main Cause of visual impairment were determined by two ophthalmologists based on the ophthalmic examinations and reported history. Moreover, we will evaluate the association between the visual impairment and different grade of DR.
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| Ages Eligible for Study: | 35 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Probability Sample |
Inclusion Criteria:
- Adults with diabetes aged 35 years and above; under archives management; residing in Shanghai.
Exclusion Criteria:
- All the study participants have difficulties of mobility or communication.
| Responsible Party: | Jiannan Huang, Principal Investigator, Shanghai Eye Disease Prevention and Treatment Center |
| ClinicalTrials.gov Identifier: | NCT03665090 |
| Other Study ID Numbers: |
YFZX2018007 |
| First Posted: | September 11, 2018 Key Record Dates |
| Last Update Posted: | September 11, 2018 |
| Last Verified: | September 2018 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | Yes |
| Plan Description: | Identified individual participant data for all primary and secondary outcome measures will be made available. |
| Supporting Materials: |
Study Protocol Statistical Analysis Plan (SAP) Informed Consent Form (ICF) Clinical Study Report (CSR) |
| Time Frame: | Data will be available with in one year of study completion. |
| Access Criteria: | Data access requests will be reviewed by an external Independent Review Panel. Requestors will be required to sign a Data Access Agreement. |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Macular Edema Diabetic Retinopathy Eye Diseases Macular Degeneration Retinal Degeneration Retinal Diseases |
Diabetic Angiopathies Vascular Diseases Cardiovascular Diseases Diabetes Complications Diabetes Mellitus Endocrine System Diseases |

