Skip to content

HLA and it Relation With the Development of Proliferative Diabetic Retinopathy in Mexican Population

HLA and it Relation With the Development of Proliferative Diabetic Retinopathy in Mexican Population

Status
Withdrawn
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00600236
Enrollment
0
Registered
2008-01-24
Start date
2004-09-30
Completion date
2008-01-31
Last updated
2024-06-03

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

Conditions

Diabetes Mellitus Type 2, Proliferative Diabetic Retinopathy

Keywords

Diabetes mellitus type 2 with 10 years of diagnosis and no diabetic retinopathy, Diabetes mellitus type 2 with 10 years of diagnosis and proliferative diabetic retinopathy

Brief summary

One of the first causes of irreversible blindness in mexican population is diabetic retinopathy which is clearly diferent between patients the time of evolution and development of retinopathy and complications. The aim of this study is to explore the inmunogenetic profile and the influence of HLA in this variations of the sickness to predict the severity of diabetic complications.

Interventions

PROCEDUREblood sample

Sponsors

Instituto Nacional de Referencia Epidemiológica (INdRE)
CollaboratorUNKNOWN
Asociación para Evitar la Ceguera en México
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Diabetes mellitus type 2 with 10 years of diagnosis and no diabetic retinopathy * Diabetes mellitus type 2 with 10 years of diagnosis and proliferative retinopathy

Exclusion criteria

* Systemic hipertension * Cardic disease * Lupus * Any kind of artritis * Allergies * Optic Neuritis * VKH * Cancer * Inmunological diseases

Countries

Mexico

Outcome results

None listed

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