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Completed Phase 3 Interventional

Triamcinolone Acetonide Plus Laser Therapy to Treat Age-Related Macular Degeneration

ClinicalTrials.gov ID: NCT00100009

Public ClinicalTrials.gov record NCT00100009. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 23, 2026, 11:59 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Multi-Center, Randomized, Phase II/III Clinical Trial to Study the Effects of Preservative-Free Triamcinolone Acetonide as an Adjunct to Photodynamic Therapy in Participants With Neovascular Age-Related Macular Degeneration

Study identification

NCT ID
NCT00100009
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
National Eye Institute (NEI)
NIH
Enrollment
30 participants

Conditions and interventions

Interventions

  • TAC-PF Drug
  • Triamcinolone Acetonide Drug

Drug

Eligibility (public fields only)

Age range
50 Years to 100 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 8, 2004
Primary completion
Not listed
Completion
Dec 19, 2006
Last update posted
Jul 1, 2017

2004 – 2006

United States locations

U.S. sites
23
U.S. states
16
U.S. cities
22
Facility City State ZIP Site status
Retina Associates Southwest (RASTA) Tucson Arizona
Doheny Eye Institute Los Angeles California
Bascom Palmer Eye Institute Miami Florida
Central Florida Retina (CFROL) Orlando Florida
Retina Associates of Florida Tampa Florida
Midwest Eye Institute Indianapolis Indiana
Elman Retina Group, P.A. - Baltimore (ERGBM) Baltimore Maryland 21237
National Institutes of Health Clinical Center, 9000 Rockville Pike Bethesda Maryland 20892
Elman Retina Group, P.A. - Pikesville (ERGPM) Pikesville Maryland 21208
University of Michigan Ann Arbor Michigan 48109-0624
VitreoRetinal Surgery (VRSMN) Center Minneapolis Minnesota
Cornell University New York New York 10021-4872
Duke University Eye Center (DUENC) Durham North Carolina 27710
Dean McGee Eye Institute (DMEIO) Oklahoma City Oklahoma
Casey Eye Institute-Portland, OR (CEIPO) Portland Oregon 97239
Retina Northwest (RNWPO) Portland Oregon
Wills Eye Hospital Philadelphia Pennsylvania
Southeastern Retina Associates (SRAKT) Knoxville Tennessee
Vanderbilt University Nashville Tennessee 37232
Texas Retina Associates Arlington Texas
Texas Retina Associates Dallas Texas
Retina Group of Washington - Fairfax (RGWFF) Fairfax Virginia 22031
University of Wisconsin Madison Wisconsin 53792

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00100009, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 1, 2017 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00100009 live on ClinicalTrials.gov.

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