Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 4 Interventional Results available

Dropless vs. Standard Drops Contralateral Eye Study

ClinicalTrials.gov ID: NCT02515045

Public ClinicalTrials.gov record NCT02515045. 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 22, 2026, 5:06 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

Comparison of Dropless Prophylaxis After Routine Phacoemulsification to Standard Drops Regimen

Study identification

NCT ID
NCT02515045
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Carolina Eyecare Physicians, LLC
Other
Enrollment
59 participants

Conditions and interventions

Conditions

Interventions

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

Drug

Eligibility (public fields only)

Age range
50 Years to 80 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 31, 2014
Primary completion
Feb 29, 2016
Completion
Feb 29, 2016
Last update posted
Feb 22, 2018

2015 – 2016

United States locations

U.S. sites
4
U.S. states
3
U.S. cities
4
Facility City State ZIP Site status
Minnesota Eye Consultants, P.A. Bloomington Minnesota 55431
Associated Eye Care Stillwater Minnesota 55082
Ophthalmic Consultants of Long Island Garden City New York 11530
Carolina Eyecare Physicians, LLC Mt. Pleasant South Carolina 29464

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 NCT02515045, 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 Feb 22, 2018 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02515045 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →