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Cornea Donor Study (CDS)

This study is ongoing, but not recruiting participants.

Sponsors and Collaborators: National Eye Institute (NEI)
Eye Bank Association of America
Bausch & Lomb, Inc.
Tissue Banks International
Vision Share, Inc.
San Diego Eye Bank
The Cornea Society
Katena Products, Inc.
ViroMed Laboratories, Inc.
Midwest Eye-Banks (Michigan Eye-Bank, Illinois Eye-Bank)
Konan Medical Corp.
Eye Bank for Sight Restoration
SightLife
Sight Society of Northeastern New York (Lions Eye Bank of Albany)
Lions Eye Bank of Oregon
Information provided by: National Eye Institute (NEI)
ClinicalTrials.gov Identifier: NCT00006411
  Purpose

The Cornea Donor Study (CDS) was designed as a prospective cohort study with the following objectives:

To determine whether the graft-failure rate over a 5-year follow-up period following corneal transplantation is the same when using corneal tissue from donors older than 65 years of age compared with tissue from younger donors.

To assess the relationship between donor/recipient ABO blood type compatibility and graft failure due to rejection.

To assess corneal endothelial cell density as an indicator of the health of the cornea and as a alternate outcome measure (in an optional Specular Microscopy Ancillary Study).


Condition Intervention
Corneal Disease
Fuch's Dystrophy
Pseudophakic Corneal Edema
Other: corneas assigned by donor age group

Genetics Home Reference related topics:   Lenz microphthalmia syndrome    oculofaciocardiodental syndrome    Peters plus syndrome   

MedlinePlus related topics:   Edema   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Other, Double Blind (Subject, Investigator, Outcomes Assessor), Parallel Assignment, Bio-equivalence Study
Official Title:   Cornea Donor Study

Further study details as provided by National Eye Institute (NEI):

Primary Outcome Measures:
  • Graft failure, defined as a regraft or a cloudy cornea that was sufficiently opaque as to compromise vision for a minimum of three consecutive months. [ Time Frame: enrollment through end of follow up ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • endothelial cell density [ Time Frame: enrollment through end of follow up ] [ Designated as safety issue: No ]

Enrollment:   1101
Study Start Date:   July 2002
Estimated Study Completion Date:   July 2013
Primary Completion Date:   December 2007 (Final data collection date for primary outcome measure)

Arms Assigned Interventions
1: Active Comparator
cornea from donor <66.0 years
Other: corneas assigned by donor age group
A web-based computer program was used to select a cornea from those available at the eye bank that met the study eligibility criteria. The program randomly selected a cornea based on a two-level minimization procedure which attempted first to balance for each surgeon the number of corneas from donors >=66 and <66 years old and then, when possible, to balance among age subgroups of 10-35, 36-50, 51-65, 66-70, and 71-75 years. The assignment was made without regard to recipient age or any other subject characteristics.
2: Active Comparator
cornea from donor >= 66.0 years
Other: corneas assigned by donor age group
A web-based computer program was used to select a cornea from those available at the eye bank that met the study eligibility criteria. The program randomly selected a cornea based on a two-level minimization procedure which attempted first to balance for each surgeon the number of corneas from donors >=66 and <66 years old and then, when possible, to balance among age subgroups of 10-35, 36-50, 51-65, 66-70, and 71-75 years. The assignment was made without regard to recipient age or any other subject characteristics.

Show detailed description  Show Detailed Description

  Eligibility
Ages Eligible for Study:   40 Years to 80 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria
  • Patients must be in the age range of 40 to 80 years.
  • Patients with corneal disease associated with endothelial dysfunction, including pseudophakic corneal edema, Fuchs' dystrophy, posterior polymorphous dystrophy, endothelial failure from another cause, interstitial keratitis (non-herpetic), or perforating corneal injury.
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00006411

Locations
United States, Florida
Jaeb Center for Health Research, Inc.    
      Tampa, Florida, United States, 33647

Sponsors and Collaborators
National Eye Institute (NEI)
Eye Bank Association of America
Bausch & Lomb, Inc.
Tissue Banks International
Vision Share, Inc.
San Diego Eye Bank
The Cornea Society
Katena Products, Inc.
ViroMed Laboratories, Inc.
Midwest Eye-Banks (Michigan Eye-Bank, Illinois Eye-Bank)
Konan Medical Corp.
Eye Bank for Sight Restoration
SightLife
Sight Society of Northeastern New York (Lions Eye Bank of Albany)
Lions Eye Bank of Oregon

Investigators
Study Chair:     Edward J Holland, MD     University of Cincinnati and Cincinnati Eye Institute    
Study Chair:     Mark J Mannis, MD     University of California, Davis    
Principal Investigator:     Roy W Beck, MD, PhD     Jaeb Center for Health Research    
Principal Investigator:     Jonathan H Lass, MD     (PI of Specular Microscopy Ancillary Study), Case Western Reserve University and University Hospitals Case Medical Center    
  More Information


NEI Clinical Studies Database  This link exits the ClinicalTrials.gov site
 

Publications of Results:

Other Publications:

Responsible Party:   Jaeb Center for Health Research ( Roy W. Beck, M.D., Ph.D. )
Study ID Numbers:   NEI-80, 5U10EY012358
First Received:   October 13, 2000
Last Updated:   April 1, 2008
ClinicalTrials.gov Identifier:   NCT00006411
Health Authority:   United States: Federal Government

Keywords provided by National Eye Institute (NEI):
cornea transplant  
corneal endothelial cell density  
moderate risk corneal diseases requiring corneal transplantation  
corneal transplantation  

Study placed in the following topic categories:
Corneal Diseases
Corneal dystrophy
Genetic Diseases, Inborn
Corneal Dystrophies, Hereditary
Eye Diseases
Corneal dystrophy, Fuchs' endothelial, 1
Fuchs' Endothelial Dystrophy
Corneal Edema
Eye Diseases, Hereditary
Edema

ClinicalTrials.gov processed this record on October 03, 2008




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