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COMPLETED NA

Intraocular Steroid After Cataract Surgery Study

NCT00478764 · View on ClinicalTrials.gov ↗

Study Summary

The use of one dose of an antibiotic and steroid injected into the eye at the end of cataract surgery is as safe and effective as the post operative use of eyedrops after cataract surgery.

Conditions Studied

Interventions

  • DRUG intraocular triamcinolone and gatifloxicin

Study Locations (1)

Wisconsin

  • Davis Duehr Dean Baraboo — Baraboo

Trial Details

FieldValue
Enrollment Target 41 participants
Start Date 2006-03
Est. Completion 2007-04
Phase NA

Sponsor

Dean Health System

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00478764

The ClinicalTrials.gov registry entry for NCT00478764 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 41 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Dean Health System, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Cataract appearing as the primary indexed condition, and to 1 intervention — of which intraocular triamcinolone and gatifloxicin is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00478764 reports 1 study location spanning 1 distinct geographic area — top geographies include Wisconsin. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00478764 about?

NCT00478764 is a clinical study titled "Intraocular Steroid After Cataract Surgery Study". The use of one dose of an antibiotic and steroid injected into the eye at the end of cataract surgery is as safe and effective as the post operative use of eyedrops after cataract surgery.

What is the current status of trial NCT00478764?

This trial is currently completed. It is a NA study. The enrollment target is 41 participants. The study started on 2006-03. Estimated completion is 2007-04.

What conditions does trial NCT00478764 study?

This clinical trial studies the following conditions: Cataract. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00478764?

The interventions under investigation include: intraocular triamcinolone and gatifloxicin (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00478764?

This trial is sponsored by Dean Health System, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00478764 being conducted?

This trial has 1 study location across Wisconsin. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial