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Genetic Markers and Proliferative Diabetic Retinopathy (REDIAGEN)

Primary Purpose

Proliferative Diabetic Retinopathy

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
genetic analysis
Sponsored by
CHU de Reims
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Proliferative Diabetic Retinopathy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • type 2 diabetic patients
  • patient with proliferative diabetic retinopathy (for arm 1)
  • patient with non proliferative diabetic retinopathy (for arm 2)
  • patient older than 18 years
  • patient consenting to participate to the study
  • patient enrolled in the national healthcare insurance program

Sites / Locations

  • Chu de Reims

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Diabetic patients with proliferative diabetic retinopathy

Diabetic patients with non proliferative diabetic retinopathy

Arm Description

Outcomes

Primary Outcome Measures

Proliferative retinopathy diabetic
diabetic retinopathy with a preretinal and / or prepapillary neovascularization diagnosed using ultra-wide-field imaging

Secondary Outcome Measures

Full Information

First Posted
August 22, 2016
Last Updated
February 10, 2021
Sponsor
CHU de Reims
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1. Study Identification

Unique Protocol Identification Number
NCT02879422
Brief Title
Genetic Markers and Proliferative Diabetic Retinopathy
Acronym
REDIAGEN
Official Title
Study of the Association Between Genetic Markers (Endothelial Lipase and Aldose Reductase) and Proliferative Diabetic Retinopathy
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
October 16, 2013 (Actual)
Primary Completion Date
March 3, 2020 (Actual)
Study Completion Date
January 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
CHU de Reims

4. Oversight

5. Study Description

Brief Summary
Type 2 Diabetes (TD2) is the leading cause of new cases of preventable blindness in these countries (and the gold-standard treatment, laser photocoagulation has proven to be effective in preventing vision loss at the end stage of eye disease due to proliferative diabetic retinopathy (PDR) that occurs in 3 to 6 % of the cases.Therefore, the ongoing search for predictive factors of sight threatening stages of diabetic retinopathy has become more important. Previous studies that have examined candidate predictive factors for diabetic eye disease have mostly focused on systemic risk factors leading to PDR. Among various clinical parameters, increased HbA1c % levels, uncontrolled blood pressure, diabetes duration, neuropathy and elevated triglycerides have been associated with PDR. Some genetic factors may also account for the development of PDR and are prospectively considered in this study .
Detailed Description
In a previous study (2011), investigators demonstrated a statistically significant relation between the Endothelial Lipase(EL) c.584C>T polymorphism and the occurrence of diabetic retinopathy in 396 french patients with diabetes type 2 (DT2) with a longitudinal follow-up. Secondly (2014) in a subgroup of 287 DT2 patients, investigators showed the impact of the EL rare T allele was consistent with a recessive mode of inheritance, with homozygotes for the rare allele differing from the carriers of the major allele. Importantly, the homozygotes for the rare T allele were more likely to present with advanced stages of diabetic retinopathy (severe non proliferative and proliferative disease) and particularly with proliferative diabetic retinopathy (PDR). Based on this model investigators decided to conduct a case-control prospective study comparing 155 french patients with DT2 with PDR (cases) and 155 french patients with DT2 without PDR (controls) on the basis of two genetic parameters: EL c.584C>T polymorphism that investigators previously studied and the C(-106)T aldose reductase polymorphism widely studied in diabetic retinopathy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Proliferative Diabetic Retinopathy

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
302 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Diabetic patients with proliferative diabetic retinopathy
Arm Type
Other
Arm Title
Diabetic patients with non proliferative diabetic retinopathy
Arm Type
Other
Intervention Type
Genetic
Intervention Name(s)
genetic analysis
Primary Outcome Measure Information:
Title
Proliferative retinopathy diabetic
Description
diabetic retinopathy with a preretinal and / or prepapillary neovascularization diagnosed using ultra-wide-field imaging
Time Frame
Day 0

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: type 2 diabetic patients patient with proliferative diabetic retinopathy (for arm 1) patient with non proliferative diabetic retinopathy (for arm 2) patient older than 18 years patient consenting to participate to the study patient enrolled in the national healthcare insurance program
Facility Information:
Facility Name
Chu de Reims
City
Reims
ZIP/Postal Code
51092
Country
France

12. IPD Sharing Statement

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Genetic Markers and Proliferative Diabetic Retinopathy

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