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Corneal Lesions in Intensive Care Unit (ICU) Clinical Trial for Proposing Interventions and Evaluating Outcomes of Nursing in the Adult Intensive Care Center Clinical Trial for Proposing Interventions and Evaluating Outcomes of Nursing in the Adult Intensive Care Center

NCT02293876 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 360

Last updated 2014-11-19

No results posted yet for this study

Summary

The purpose of the study is find out the better measure to achieve corneal protection in an Intensive Care Unit.

Conditions

  • Keratitis
  • Corneal Ulcer

Interventions

DEVICE

LACRIBELL®

Hypromellose and dextran based eyedrop, used in the treatment of dry eye.

DEVICE

LIPOSIC®

Carbomer and Sorbitol based gel, used in the treatment of dry eye.

DEVICE

Glad wrap

A clear plastic wrap occluding eye and orbital area, turning the space into a moisture chamber.

Sponsors & Collaborators

  • Conselho Nacional de Desenvolvimento Científico e Tecnológico

    collaborator OTHER_GOV

  • Fundação de Amparo à Pesquisa do estado de Minas Gerais

    collaborator OTHER

  • Hospital Risoleta Tolentino Neves

    lead OTHER

Principal Investigators

  • Andreza Werli-Alvarenga, RN, MD, PhD · Hospital Risoleta Tolentino Neves

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
FACTORIAL

Eligibility

Min Age
18 Years
Max Age
93 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-04-30
Primary Completion
2014-04-30
Completion
2014-11-30

Countries

  • Brazil

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 NCT02293876 on ClinicalTrials.gov