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Completed Phase 3 Interventional

DY001: Safety and Effectiveness of DYME as an Agent for Selective Staining of the Anterior Capsule During Cataract Surgery

ClinicalTrials.gov ID: NCT00596583

Public ClinicalTrials.gov record NCT00596583. 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 Sep 3, 2026, 7:25 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

AQNA-DY001: A Double-Masked, Randomized Study of the Safety and Effectiveness of DYME as an Agent for Selective Staining of the Anterior Capsule During Cataract Surgery

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The primary objective of this study is to test the hypothesis that DYME is safe and effective as a drug to facilitate continuous curvilinear capsulorhexis (CCC) by selectively staining the anterior capsule. Secondary objectives are to compare the safety and effectiveness of DYME to that of a smaller dose of the same API.

Study identification

NCT ID
NCT00596583
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Aqumen Biopharmaceuticals, N.A.
Industry
Enrollment
300 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Mar 31, 2007
Primary completion
Apr 30, 2008
Completion
Apr 30, 2008
Last update posted
Mar 1, 2009

2007 – 2008

United States locations

U.S. sites
17
U.S. states
10
U.S. cities
16
Facility City State ZIP Site status
McDonald Eye Associates Fayetteville Arkansas 72703
Peace Laser Eye Center Inglewood California 90301
Capitol City Surgery Center Sacramento California 95815
The Eye Institute of West Florida Largo Florida 33770
Center for Excellence in Eye Care Miami Florida 33176
Eye Surgeons of Indiana Indianapolis Indiana 46256
Silverstein Eye Centers Kansas City Missouri 64133
St. John's Clinic Eye Specialists Springfield Missouri 65804
Ballas Surgery Center St Louis Missouri 63141
Wills Eye Surgery Center Cherry Hill New Jersey 08002
Brar-Parekh Eye Associates Woodland Park New Jersey 07424
Island Eye Surgicenter Carle Place New York 11514
The Ohio State University Hospital Columbus Ohio 43210
Eye Care Specialists Kingston Pennsylvania 18704
Wills Eye Surgery Center Philadelphia Pennsylvania 19107
Wills Surgery Center Philadelphia Pennsylvania 19145
SMDV Surgery Center Madison Wisconsin 53715

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00596583, 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 Mar 1, 2009 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00596583 live on ClinicalTrials.gov.

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