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COMPLETED Phase 4

Dropless vs. Standard Drops Contralateral Eye Study

NCT02515045 · View on ClinicalTrials.gov ↗

Study Summary

To compare the use of an injectable compound containing an antibiotic and an anti-inflammatory at time of cataract surgery to standard of care that is the use 3 different topical medications to prevent inflammation and infection after routine cataract surgery.

Conditions Studied

Interventions

  • DRUG TriMoxiVanc
  • DRUG Moxifloxacin HCl 0.5%
  • DRUG Ilevro
  • DRUG Prednisolone acetate 1%

Study Locations (4)

Minnesota

  • Minnesota Eye Consultants, P.A. — Bloomington
  • Associated Eye Care — Stillwater

New York

  • Ophthalmic Consultants of Long Island — Garden City

South Carolina

  • Carolina Eyecare Physicians, LLC — Mt. Pleasant

Trial Details

FieldValue
Enrollment Target 59 participants
Start Date 2015-01
Est. Completion 2016-03
Phase Phase 4

Sponsor

Carolina Eyecare Physicians

8 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02515045

The ClinicalTrials.gov registry entry for NCT02515045 describes a study currently listed as completed. It is categorized as Phase 4, 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 59 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Carolina Eyecare Physicians, which has 8 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 4 interventions — of which TriMoxiVanc 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: NCT02515045 reports 4 study locations spanning 3 distinct geographic areas — top geographies include Minnesota, New York, South Carolina. 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 NCT02515045 about?

NCT02515045 is a clinical study titled "Dropless vs. Standard Drops Contralateral Eye Study". To compare the use of an injectable compound containing an antibiotic and an anti-inflammatory at time of cataract surgery to standard of care that is the use 3 different topical medications to prevent inflammation and infection after routine cataract surgery.

What is the current status of trial NCT02515045?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 59 participants. The study started on 2015-01. Estimated completion is 2016-03.

What conditions does trial NCT02515045 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 NCT02515045?

The interventions under investigation include: TriMoxiVanc (DRUG), Moxifloxacin HCl 0.5% (DRUG), Ilevro (DRUG), Prednisolone acetate 1% (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02515045?

This trial is sponsored by Carolina Eyecare Physicians, which has 8 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02515045 being conducted?

This trial has 4 study locations across Minnesota, New York, South Carolina. 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