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Evaluating How the Treatments in the Action to Control Cardiovascular Risk in Diabetes (ACCORD) Study Affect Diabetic Retinopathy (The ACCORD Eye Study)

Primary Purpose

Diabetic Retinopathy

Status
Completed
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
Hypoglycemic Agents
Standard glycemia control
Intensive BP treatment
Standard BP control
Fenofibrate
Simvastatin
Placebo
Sponsored by
National Heart, Lung, and Blood Institute (NHLBI)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Diabetic Retinopathy focused on measuring Type 2 Diabetes Mellitus, Cardiovascular Diseases

Eligibility Criteria

40 Years - 79 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Participating in the ACCORD study

Exclusion Criteria:

  • Has had laser photocoagulation for DR
  • Has had vitrectomy surgery for DR

Sites / Locations

  • The Berman Center for Clinical Research
  • Columbia University
  • Wake Forest University Health Sciences
  • Case Western Reserve University
  • Veterans Affairs
  • University of Washington
  • McMaster University

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm Type

Experimental

Active Comparator

Experimental

Active Comparator

Experimental

Placebo Comparator

Arm Label

Intensive glycemia control

Standard glycemia control

Intensive BP control

Standard BP control

Fibrate

Fibrate Placebo

Arm Description

A strategy of intensive glycemia treatment to HbA1c less than 6%

A strategy of multiple drugs to treat HbA1c to 7.0% - 7.9%

A strategy of BP treatment for SBP less than 120 mm Hg

A strategy of BP treatment for SBP less than 140 mm Hg

Blinded fenofibrate + simvastatin 20-40 mg/d

Blinded placebo + simvastatin 20-40 mg/d

Outcomes

Primary Outcome Measures

Number of Participants With Progression of Diabetic Retinopathy of at Least 3 Stages on the Early Treatment Diabetic Retinopathy Study (ETDRS) Scale, or Development of Proliferative Diabetic Retinopathy Necessitating Photocoagulation Therapy or Vitrectomy
Diabetic retinopathy status was defined according to the eye with the highest level on the ETDRS Final Severity Scale for Persons, as follows: no diabetic retinopathy, a level of less than 20; mild diabetic retinopathy, a level of 20; moderate nonproliferative diabetic retinopathy (NPDR), a level above 20 but less than 53; severe diabetic retinopathy, a level of 53 but less than 60; and proliferative diabetic retinopathy (PDR), a level of 60 or higher.

Secondary Outcome Measures

Loss of Visual Acuity
Cataract Extraction
Development or Progression of Macular Edema

Full Information

First Posted
October 9, 2007
Last Updated
June 27, 2018
Sponsor
National Heart, Lung, and Blood Institute (NHLBI)
Collaborators
National Eye Institute (NEI)
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1. Study Identification

Unique Protocol Identification Number
NCT00542178
Brief Title
Evaluating How the Treatments in the Action to Control Cardiovascular Risk in Diabetes (ACCORD) Study Affect Diabetic Retinopathy (The ACCORD Eye Study)
Official Title
Action to Control Cardiovascular Risk in Diabetes (ACCORD) Eye Study
Study Type
Interventional

2. Study Status

Record Verification Date
October 2016
Overall Recruitment Status
Completed
Study Start Date
October 2003 (undefined)
Primary Completion Date
December 2009 (Actual)
Study Completion Date
December 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Heart, Lung, and Blood Institute (NHLBI)
Collaborators
National Eye Institute (NEI)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Diabetic retinopathy (DR) is an eye disease that can occur in people with diabetes and can cause poor vision or blindness. The Action to Control Cardiovascular Risk in Diabetes (ACCORD) study is examining the effect of various treatments on cardiovascular disease in people with diabetes. This current study will examine the effects of the ACCORD treatments on the progression of DR in people participating in the ACCORD study.
Detailed Description
DR is the most common diabetic eye disease and is the leading cause of blindness in adults in the United States. It is caused by damage to the blood vessels of the retina, which is the light-sensitive outer layer of the eye. Retinal blood vessels are often affected by the high blood sugar levels associated with diabetes. Older people have an increased risk of developing DR; however, DR is likely to occur earlier and be more severe in anyone who has poorly controlled diabetes. Almost everyone who has had diabetes for more than 30 years will eventually show signs of DR. Symptoms of DR include poor night vision, seeing spots in front of the eyes, blurred vision, and blindness. The ACCORD study is a study that is examining the effects of different treatments on cardiovascular disease in people with diabetes. Participants in the ACCORD study will receive one of eight different combinations of treatment, including blood sugar control, blood pressure control, and cholesterol-controlling medication. This study will enroll participants in the ACCORD study and will examine the effects of the study treatments on DR. The results from this study may be used to develop new treatments to help prevent diabetes-related blindness. Study visits will occur at baseline and Year 4. At each study visit, participants will have an eye exam and specialized fundus photographs taken of the back of the eye and retina.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Retinopathy
Keywords
Type 2 Diabetes Mellitus, Cardiovascular Diseases

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Factorial Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
3472 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intensive glycemia control
Arm Type
Experimental
Arm Description
A strategy of intensive glycemia treatment to HbA1c less than 6%
Arm Title
Standard glycemia control
Arm Type
Active Comparator
Arm Description
A strategy of multiple drugs to treat HbA1c to 7.0% - 7.9%
Arm Title
Intensive BP control
Arm Type
Experimental
Arm Description
A strategy of BP treatment for SBP less than 120 mm Hg
Arm Title
Standard BP control
Arm Type
Active Comparator
Arm Description
A strategy of BP treatment for SBP less than 140 mm Hg
Arm Title
Fibrate
Arm Type
Experimental
Arm Description
Blinded fenofibrate + simvastatin 20-40 mg/d
Arm Title
Fibrate Placebo
Arm Type
Placebo Comparator
Arm Description
Blinded placebo + simvastatin 20-40 mg/d
Intervention Type
Drug
Intervention Name(s)
Hypoglycemic Agents
Intervention Description
Multiple drugs including insulins and oral hypoglycemia agents for HbA1c less than 6%
Intervention Type
Drug
Intervention Name(s)
Standard glycemia control
Intervention Description
A strategy of glycemia drugs for HbA1c 7% - 7.9%
Intervention Type
Drug
Intervention Name(s)
Intensive BP treatment
Intervention Description
A strategy of multiple BP agents to reduce SBP less than 120 mm Hg
Intervention Type
Drug
Intervention Name(s)
Standard BP control
Intervention Description
A strategy of BP drugs for SBP less than 140 mm Hg
Intervention Type
Drug
Intervention Name(s)
Fenofibrate
Intervention Description
Blinded fenofibrate
Intervention Type
Drug
Intervention Name(s)
Simvastatin
Intervention Description
Simvastatin 20-40 mg/d
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
Number of Participants With Progression of Diabetic Retinopathy of at Least 3 Stages on the Early Treatment Diabetic Retinopathy Study (ETDRS) Scale, or Development of Proliferative Diabetic Retinopathy Necessitating Photocoagulation Therapy or Vitrectomy
Description
Diabetic retinopathy status was defined according to the eye with the highest level on the ETDRS Final Severity Scale for Persons, as follows: no diabetic retinopathy, a level of less than 20; mild diabetic retinopathy, a level of 20; moderate nonproliferative diabetic retinopathy (NPDR), a level above 20 but less than 53; severe diabetic retinopathy, a level of 53 but less than 60; and proliferative diabetic retinopathy (PDR), a level of 60 or higher.
Time Frame
Measured at Year 4
Secondary Outcome Measure Information:
Title
Loss of Visual Acuity
Time Frame
Measured at Year 4
Title
Cataract Extraction
Time Frame
Measured at Year 4
Title
Development or Progression of Macular Edema
Time Frame
Measured at Year 4

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
79 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Participating in the ACCORD study Exclusion Criteria: Has had laser photocoagulation for DR Has had vitrectomy surgery for DR
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Walter T. Ambrosius, PhD
Organizational Affiliation
Wake Forest University Health Sciences
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Emily Y. Chew, MD
Organizational Affiliation
National Eye Institute (NEI)
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Berman Center for Clinical Research
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55404
Country
United States
Facility Name
Columbia University
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States
Facility Name
Wake Forest University Health Sciences
City
Winston-Salem
State/Province
North Carolina
ZIP/Postal Code
27157
Country
United States
Facility Name
Case Western Reserve University
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44106-4951
Country
United States
Facility Name
Veterans Affairs
City
Memphis
State/Province
Tennessee
ZIP/Postal Code
38104-2193
Country
United States
Facility Name
University of Washington
City
Seattle
State/Province
Washington
ZIP/Postal Code
98109
Country
United States
Facility Name
McMaster University
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8L 2X2
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
17599420
Citation
Chew EY, Ambrosius WT, Howard LT, Greven CM, Johnson S, Danis RP, Davis MD, Genuth S, Domanski M; ACCORD Study Group. Rationale, design, and methods of the Action to Control Cardiovascular Risk in Diabetes Eye Study (ACCORD-EYE). Am J Cardiol. 2007 Jun 18;99(12A):103i-111i. doi: 10.1016/j.amjcard.2007.03.028. Epub 2007 Apr 13.
Results Reference
background
PubMed Identifier
20587587
Citation
ACCORD Study Group; ACCORD Eye Study Group; Chew EY, Ambrosius WT, Davis MD, Danis RP, Gangaputra S, Greven CM, Hubbard L, Esser BA, Lovato JF, Perdue LH, Goff DC Jr, Cushman WC, Ginsberg HN, Elam MB, Genuth S, Gerstein HC, Schubart U, Fine LJ. Effects of medical therapies on retinopathy progression in type 2 diabetes. N Engl J Med. 2010 Jul 15;363(3):233-44. doi: 10.1056/NEJMoa1001288. Epub 2010 Jun 29. Erratum In: N Engl J Med. 2011 Jan 13;364(2):190. N Engl J Med. 2012 Dec 20;367(25):2458.
Results Reference
result
PubMed Identifier
27289122
Citation
Action to Control Cardiovascular Risk in Diabetes Follow-On (ACCORDION) Eye Study Group and the Action to Control Cardiovascular Risk in Diabetes Follow-On (ACCORDION) Study Group. Persistent Effects of Intensive Glycemic Control on Retinopathy in Type 2 Diabetes in the Action to Control Cardiovascular Risk in Diabetes (ACCORD) Follow-On Study. Diabetes Care. 2016 Jul;39(7):1089-100. doi: 10.2337/dc16-0024. Epub 2016 Jun 11.
Results Reference
derived
PubMed Identifier
25172198
Citation
Chew EY, Davis MD, Danis RP, Lovato JF, Perdue LH, Greven C, Genuth S, Goff DC, Leiter LA, Ismail-Beigi F, Ambrosius WT; Action to Control Cardiovascular Risk in Diabetes Eye Study Research Group. The effects of medical management on the progression of diabetic retinopathy in persons with type 2 diabetes: the Action to Control Cardiovascular Risk in Diabetes (ACCORD) Eye Study. Ophthalmology. 2014 Dec;121(12):2443-51. doi: 10.1016/j.ophtha.2014.07.019. Epub 2014 Aug 29.
Results Reference
derived
PubMed Identifier
22709833
Citation
Wong TY, Simo R, Mitchell P. Fenofibrate - a potential systemic treatment for diabetic retinopathy? Am J Ophthalmol. 2012 Jul;154(1):6-12. doi: 10.1016/j.ajo.2012.03.013.
Results Reference
derived
PubMed Identifier
20212201
Citation
Ambrosius WT, Danis RP, Goff DC Jr, Greven CM, Gerstein HC, Cohen RM, Riddle MC, Miller ME, Buse JB, Bonds DE, Peterson KA, Rosenberg YD, Perdue LH, Esser BA, Seaquist LA, Felicetta JV, Chew EY; ACCORD Study Group. Lack of association between thiazolidinediones and macular edema in type 2 diabetes: the ACCORD eye substudy. Arch Ophthalmol. 2010 Mar;128(3):312-8. doi: 10.1001/archophthalmol.2009.310.
Results Reference
derived
Links:
URL
http://www.accordtrial.org/
Description
Click here for the ACCORD Study Web site

Learn more about this trial

Evaluating How the Treatments in the Action to Control Cardiovascular Risk in Diabetes (ACCORD) Study Affect Diabetic Retinopathy (The ACCORD Eye Study)

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