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The Early Treatment for Retinopathy of Prematurity Study (ETROP)

Primary Purpose

Retinopathy of Prematurity

Status
Unknown status
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
retinal ablation
Sponsored by
National Eye Institute (NEI)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Retinopathy of Prematurity

Eligibility Criteria

0 Years - 42 Days (Child)All SexesDoes not accept healthy volunteers

Infants <1251 grams birthweight born at participating centers and/or examined by 42 days of life are eligible. The early treatment trial requires that an infant have prethreshold retinopathy of prematurity (ROP).

Sites / Locations

  • Stanford University School of Medicine
  • Smith-Kettlewell Eye Research Institute
  • UIC Eye Center Department of Ophthalmology and Visual Sciences The Lions of Illinois Eye Research Institute
  • Indiana University Department of Pediatrics
  • University of Louisville Health Sciences Center
  • Tulane University Medical Center
  • University of Maryland School of Medicine
  • The Zanvyl Krieger Children's Eye Center
  • Tufts University School of Medicine Department of Pediatrics
  • Pediatric Ophthalmology Associates, PC
  • University of Minnesota
  • Cardinal Glennon Children's Hospital Neonatology Office
  • The Children's Hospital of Buffalo Department of Ophthalmology
  • Edward S. Harkness Eye Institute
  • University of Rochester Medical Center
  • Eastern Long Island Retina Associate
  • Duke University Eye Center
  • Columbus Children's Hospital
  • The Dean A. McGee Eye Institute
  • Oregon Health Sciences University Casey Eye Institute
  • The Children's Hospital of Philadelphia Division of Pediatric Ophthalmology
  • Magee-Women's Hospital
  • Medical University of South Carolina
  • Baylor College of Medicine Feigin Center
  • University of Texas Health Science Center at San Antonio
  • John Moran Eye Center University of Utah Health Sciences Center

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
November 28, 2001
Last Updated
June 23, 2005
Sponsor
National Eye Institute (NEI)
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1. Study Identification

Unique Protocol Identification Number
NCT00027222
Brief Title
The Early Treatment for Retinopathy of Prematurity Study (ETROP)
Official Title
The Early Treatment for Retinopathy of Prematurity Study (ETROP)
Study Type
Interventional

2. Study Status

Record Verification Date
December 2003
Overall Recruitment Status
Unknown status
Study Start Date
October 2001 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
National Eye Institute (NEI)

4. Oversight

5. Study Description

Brief Summary
The goal of the Early Treatment for Retinopathy of Prematurity Study (ETROP) is to test the hypothesis that earlier treatment in carefully selected cases will result in an overall better visual outcome than treatment at the conventional CRYO-ROP threshold point in the disease.
Detailed Description
At age 5 1/2 years, the oldest age for which follow-up data are available, children with threshold ROP who were enrolled in the Cryotherapy for Retinopathy of Prematurity (CRYO-ROP) -- Outcome Study showed fewer treated eyes (31.5 percent) than control eyes (48 percent) that were blind (P<0.001). Of those eyes that had a favorable structural outcome, with or without retinal ablation (cryotherapy to destroy the fringe of the retina through freezing), only a small percentage had best corrected visual acuity better than or equal to 20/40 at age 5 1/2 years (13 percent in the treated group; 17 percent in the untreated control group (P=0.19)). Among the 1398 followed from the 5 large natural history centers of the CRYO-ROP follow-up study, children with retinal residua of ROP (structural changes) had measurable visual acuity that was severly affected and tended to worsen with age. The CRYO-ROP Study proved conclusively that peripheral retinal ablation improves the chances of avoiding blindness, but at least 80 percent of eyes are left with acuity less than 20/40. Two concerns emerged from the CRYO-ROP extensive study on the natural history of ROP and treatment of threshold ROP. The first of these is failure of peripheral retinal ablation to eliminate all, or nearly all cases, of retinal detachment due to ROP. In the CRYO-ROP Study, 26 percent of eyes with threshold disease in zone II and 78 percent of eyes with zone I threshold disease had an unfavorable structural outcome despite treatment. The second concern is that most children who developed threshold ROP disease had visual acuity worse than 20/40 even if the eye had a favorable structural outcome. Since no other treatment has yet been shown to be effective in preventing blindness from ROP, retinal ablation remains the treatment of choice. The ETROP Study will test whether earlier treatment is more effective than treatment at threshold in improving functional (visual acuity) outcome following ROP, as well as determining whether earlier treatment decreases the probability of an unfavorable structural outcome. Earlier treatment is defined as retinal ablation administered to the avascular retina when an eye reaches high risk prethreshold retinopathy of prematurity (ROP). Prethreshold indicates any Zone I ROP; or Zone II stage 2 with plus disease, or stage 3; or Zone II with less than 5 contiguous or 8 cumulative clock hours of stage 3 ROP with plus disease. Recognizing that a substantial number of eyes undergo spontaneous resolution of ROP, eyes will be randomized to early treatment only when high risk for an unfavorable visual acuity outcome is identified. High risk will be determined using a risk model analysis program based on longitudinal natural history data obtained from the CRYO-ROP study. This model integrates risk factors to assign a risk of progression to blindness without treatment. These factors include birth weight, gestational age, ethnicity, singleton/multiple status, outborn status, Zone on first exam, severity of ROP and rate of progression of ROP. When an infant develops prethreshold ROP and greater than or equal to 15 percent risk of unfavorable outcome, randomization to early treatment of one eye will occur. Visual acuity outcome will be measured by masked observers after wearing best correction using the Teller Acuity Card Procedure at 9 months corrected age.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3

8. Arms, Groups, and Interventions

Intervention Type
Procedure
Intervention Name(s)
retinal ablation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
0 Years
Maximum Age & Unit of Time
42 Days
Accepts Healthy Volunteers
No
Eligibility Criteria
Infants <1251 grams birthweight born at participating centers and/or examined by 42 days of life are eligible. The early treatment trial requires that an infant have prethreshold retinopathy of prematurity (ROP).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
William V. Good, M.D.
Organizational Affiliation
Smith-Kettlewell Eye Research Institute
Official's Role
Study Chair
Facility Information:
Facility Name
Stanford University School of Medicine
City
Palo Alto
State/Province
California
ZIP/Postal Code
94304
Country
United States
Facility Name
Smith-Kettlewell Eye Research Institute
City
San Francisco
State/Province
California
ZIP/Postal Code
94115-1813
Country
United States
Facility Name
UIC Eye Center Department of Ophthalmology and Visual Sciences The Lions of Illinois Eye Research Institute
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60612-724
Country
United States
Facility Name
Indiana University Department of Pediatrics
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46002-2119
Country
United States
Facility Name
University of Louisville Health Sciences Center
City
Louisville
State/Province
Kentucky
ZIP/Postal Code
40202-1594
Country
United States
Facility Name
Tulane University Medical Center
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70112-2699
Country
United States
Facility Name
University of Maryland School of Medicine
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21201-1595
Country
United States
Facility Name
The Zanvyl Krieger Children's Eye Center
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21287
Country
United States
Facility Name
Tufts University School of Medicine Department of Pediatrics
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02111
Country
United States
Facility Name
Pediatric Ophthalmology Associates, PC
City
Dearborn
State/Province
Michigan
ZIP/Postal Code
48124
Country
United States
Facility Name
University of Minnesota
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55455-0591
Country
United States
Facility Name
Cardinal Glennon Children's Hospital Neonatology Office
City
St. Louis
State/Province
Missouri
ZIP/Postal Code
63104
Country
United States
Facility Name
The Children's Hospital of Buffalo Department of Ophthalmology
City
Buffalo
State/Province
New York
ZIP/Postal Code
14222-2099
Country
United States
Facility Name
Edward S. Harkness Eye Institute
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States
Facility Name
University of Rochester Medical Center
City
Rochester
State/Province
New York
ZIP/Postal Code
14642
Country
United States
Facility Name
Eastern Long Island Retina Associate
City
Shirley
State/Province
New York
ZIP/Postal Code
111967
Country
United States
Facility Name
Duke University Eye Center
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27710
Country
United States
Facility Name
Columbus Children's Hospital
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43205
Country
United States
Facility Name
The Dean A. McGee Eye Institute
City
Oklahoma City
State/Province
Oklahoma
ZIP/Postal Code
73104
Country
United States
Facility Name
Oregon Health Sciences University Casey Eye Institute
City
Portland
State/Province
Oregon
ZIP/Postal Code
97201-4197
Country
United States
Facility Name
The Children's Hospital of Philadelphia Division of Pediatric Ophthalmology
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104-4399
Country
United States
Facility Name
Magee-Women's Hospital
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213-3180
Country
United States
Facility Name
Medical University of South Carolina
City
Charleston
State/Province
South Carolina
ZIP/Postal Code
29425-2236
Country
United States
Facility Name
Baylor College of Medicine Feigin Center
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Facility Name
University of Texas Health Science Center at San Antonio
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78229-3900
Country
United States
Facility Name
John Moran Eye Center University of Utah Health Sciences Center
City
Salt Lake City
State/Province
Utah
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
22892757
Citation
Wallace DK, Bremer DL, Good WV, Fellows R, Summers CG, Tung B, Hardy RJ. Correlation of recognition visual acuity with posterior retinal structure in advanced retinopathy of prematurity. Arch Ophthalmol. 2012 Dec;130(12):1512-6. doi: 10.1001/archophthalmol.2012.2118.
Results Reference
derived
PubMed Identifier
22232483
Citation
Good WV, Hardy RJ, Wallace DK, Bremer D, Rogers DL, Siatkowski RM, De Becker I, Summers CG, Fellows R, Tung B, Palmer EA. beta-Blocking and racial variation in the severity of retinopathy of prematurity. Arch Ophthalmol. 2012 Jan;130(1):117-8. doi: 10.1001/archopht.130.1.117. No abstract available.
Results Reference
derived
PubMed Identifier
22153396
Citation
VanderVeen DK, Bremer DL, Fellows RR, Hardy RJ, Neely DE, Palmer EA, Rogers DL, Tung B, Good WV; Early Treatment for Retinopathy of Prematurity Cooperative Group. Prevalence and course of strabismus through age 6 years in participants of the Early Treatment for Retinopathy of Prematurity randomized trial. J AAPOS. 2011 Dec;15(6):536-40. doi: 10.1016/j.jaapos.2011.07.017.
Results Reference
derived
PubMed Identifier
21746974
Citation
Early Treatment for Retinopathy of Prematurity Cooperative Group; Dobson V, Quinn GE, Summers CG, Hardy RJ, Tung B, Good WV. Grating visual acuity results in the early treatment for retinopathy of prematurity study. Arch Ophthalmol. 2011 Jul;129(7):840-6. doi: 10.1001/archophthalmol.2011.143.
Results Reference
derived
PubMed Identifier
21320954
Citation
Quinn GE, Dobson V, Hardy RJ, Tung B, Palmer EA, Good WV; Early Treatment for Retinopathy of Prematurity Cooperative Group. Visual field extent at 6 years of age in children who had high-risk prethreshold retinopathy of prematurity. Arch Ophthalmol. 2011 Feb;129(2):127-32. doi: 10.1001/archophthalmol.2010.360.
Results Reference
derived
PubMed Identifier
20385942
Citation
Christiansen SP, Dobson V, Quinn GE, Good WV, Tung B, Hardy RJ, Baker JD, Hoffman RO, Reynolds JD, Rychwalski PJ, Shapiro MJ; Early Treatment for Retinopathy of Prematurity Cooperative Group. Progression of type 2 to type 1 retinopathy of prematurity in the Early Treatment for Retinopathy of Prematurity Study. Arch Ophthalmol. 2010 Apr;128(4):461-5. doi: 10.1001/archophthalmol.2010.34.
Results Reference
derived
PubMed Identifier
20385926
Citation
Early Treatment for Retinopathy of Prematurity Cooperative Group; Good WV, Hardy RJ, Dobson V, Palmer EA, Phelps DL, Tung B, Redford M. Final visual acuity results in the early treatment for retinopathy of prematurity study. Arch Ophthalmol. 2010 Jun;128(6):663-71. doi: 10.1001/archophthalmol.2010.72. Epub 2010 Apr 12. Erratum In: Arch Ophthalmol. 2012 Jun;130(6):719.
Results Reference
derived

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The Early Treatment for Retinopathy of Prematurity Study (ETROP)

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