None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: All adults who are > 40 years of age (special community groups also will contain only adult population) Ability to give informed consent Local residents of indian origin
Exclusion criteria
Exclusion criteria: Subjects who do not have the ability to give consent Vulnerable adults in whom it may not be possible to carry out all tests Pregnant and breast feeding women Anyone in the opinion of the health worker deemed too ill to be screened. Current participation in intervention trials with investigational medicinal products
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate the diagnostic accuracy of various tests (Table 4) that can diagnose prediabetes and diabetes, retinopathy and a combination of both microvascular and macrovascular complications to be used as screening models for holistic screening for diabetes and its complicationsTimepoint: The screening is aimed to be completed in 18 to 36 months. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1)Evaluate the clinical and cost-effectiveness of various models including the trade-offs of using an economically viable model compared to an ideal model. 2)Perform further statistical modelling to refine stratification and risk prediction 3)A process evaluation will be done in accordance with the MRC guidance and Re-aim theoretical frameworkTimepoint: The screening is aimed to be completed in 18 to 36 months. | — |
Countries
India, United Kingdom
Contacts
Sankara Nethralaya