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Complications of Age-Related Macular Degeneration Prevention Trial (CAPT)
This study has been completed.
Study NCT00000167   Information provided by National Eye Institute (NEI)
First Received: September 23, 1999   Last Updated: December 21, 2007   History of Changes

September 23, 1999
December 21, 2007
May 1999
 
Change in visual acuity (3-line loss) [ Time Frame: 5 years ] [ Designated as safety issue: No ]
Change in visual acuity
Complete list of historical versions of study NCT00000167 on ClinicalTrials.gov Archive Site
  • Incidence of complications of AMD such as neovascularization, serous detachment of the pigment epithelium, and geographic atrophy [ Time Frame: 5 years ] [ Designated as safety issue: No ]
  • Changes in contrast threshold and critical print size for reading [ Time Frame: 5 years ] [ Designated as safety issue: No ]
  • Incidence of complications of AMD such as neovascularization, serous detachment of the pigment epithelium, and geographic atrophy
  • Changes in contrast threshold and critical print size for reading
 
Complications of Age-Related Macular Degeneration Prevention Trial
Complications of Age-Related Macular Degeneration Prevention Trial (CAPT)

To determine whether application of low-intensity laser treatment of eyes with drusen in the macula can prevent later complications of age-related macular degeneration and thereby preserve visual function.

Complications of age-related macular degeneration (AMD) are the leading cause of severe vision loss among people aged 65 and over in the United States and many Western countries. Most, (approximately 90 percent), of this vision loss is due to the neovascular (or wet) form of AMD. The word neovascular describes the development of new, abnormal blood vessels in the back of the eye. Unfortunately, the majority of these new vessels are not amenable to currently available treatments.

The first sign that an eye may develop AMD is the presence of drusen, yellowish deposits under the retina. Current data suggests that eyes with large drusen are at increased risk for developing the vision threatening complications of AMD. Since the 1970s investigators have reported consistently that laser photocoagulation causes a reduction in large drusen. However, results of the effects of laser treatment on preventing later complications of AMD have been less consistent and based on relatively small numbers of patients.

Further study into the ability of a treatment to prevent vision loss from the advanced forms of AMD would have profound public health implications. A treatment that could reduce the risk of developing neovascularization by 30 percent might reduce the risk of blindness from AMD by one half. The Complications of Age-related Macular Degeneration Prevention Trial (CAPT) will assess whether treating drusen by laser photocoagulation reduces the risk of loss of visual acuity.

The CAPT is a multi-center, prospective, randomized clinical trial designed to assess the safety and effectiveness of low-intensity laser treatment in preventing vision loss among patients with large drusen in both eyes. A total of 1052 participants were enrolled in the study. Participants had one eye randomly assigned to laser treatment performed by a CAPT-certified ophthalmologist. The other eye was not treated. Both eyes were observed carefully for any changes for a period of five years. The effectiveness of the treatment was assessed using the following criteria:

Change in visual acuity (primary outcome measure of the study)

Incidence of complications of AMD such as neovascularization, serous detachment of the pigment epithelium, and geographic atrophy

Changes in contrast threshold and critical print size for reading

Quality of life assessments for patients, using the Visual Function Questionnaire 25 (VFQ-25), were conducted at the time of enrollment and at 5 years.

STUDY RESULTS:

Follow-up of patients was excellent; less than 3% of visual acuity examinations were missed. At 5 years, 188 (20.5%) treated eyes and 188 (20.5%) observed eyes had visual acuity scores ≥3 lines worse than at the initial visit (p= 1.00). The cumulative 5-year incidence rates for treated and observed eyes for CNV were 13.3% and 13.3% (p=0.95), respectively; and for GA were 7.4% and 7.8% (p=0.64), respectively. The contrast threshold doubled in 23.9% of treated eyes and in 20.5% of observed eyes (p=0.40). The critical print size doubled in 29.6% of treated eyes and in 28.4% of observed eyes (p=0.70). Seven (0.7%) treated eyes and 14 (1.3%) observed eyes had an adverse event of a ≥6 -line loss in visual acuity in the absence of late age-related macular degeneration or cataract.

As applied in CAPT, low intensity laser treatment did not demonstrate a clinically significant benefit on vision in eyes of people with bilateral large drusen.

Phase III
Interventional
Prevention, Randomized, Single Blind (Outcomes Assessor), Placebo Control, Single Group Assignment, Safety/Efficacy Study
Macular Degeneration
Procedure: Low-Intensity Laser Treatment
Experimental: Laser treatment
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Completed
1052
June 2006
 

Patients eligible for CAPT can be either male or female and meet the following criteria:

Age at least 50 years old

Vision in each eye must measure 20/40 or better.

At least 10 large drusen in each eye

Available for follow-up examinations for 5 years after enrollment

Final eligibility is determined through a detailed eye examination by a CAPT-certified ophthalmologist.

Both
50 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00000167
Natalie Kurinij, NEI
NEI-70
National Eye Institute (NEI)
 
Study Chair: Stuart L Fine, MD Scheie Eye Institute, The University of Pennsylvania School of Medicine
National Eye Institute (NEI)
December 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP