The Effect of Punctal Plugs on Ocular Surface After Povidone-Iodine Preparation of Intravitreal Injection

NCT03945071 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 126

Last updated 2023-12-07

No results posted yet for this study

Summary

The aim of this study is to evaluate the effectiveness of punctal plugs in reducing ocular surface (eye surface) irritation after intravitreal injections prepared by povidone-iodine 5% solution.

Conditions

  • Dry Eye Syndromes
  • Dry Eye
  • Ocular Surface Disease

Interventions

DEVICE

Punctal plug

Punctal plug will be given to subjects after intravitreal injection in half of the study subjects

Sponsors & Collaborators

  • University of Oklahoma

    lead OTHER

Principal Investigators

  • Vinay Shah, MD · University of Oklahoma

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-06-01
Primary Completion
2020-10-18
Completion
2020-10-18
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03945071 on ClinicalTrials.gov