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Defining the Conjunctival Staining Method: Instillation Volume and Time Course to Assess Staining With Lissamine Green

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Alcon

Status

Completed

Conditions

Conjunctival Staining

Treatments

Other: 2.5/5.0/10.0 µL lissamine green

Study type

Observational

Funder types

Industry

Identifiers

NCT00768898
M-08-01

Details and patient eligibility

About

The purpose of this study is to determine the correct volume of lissamine green to use when assessing conjunctival staining, and to determine the time course needed to evaluate conjunctival staining after lissamine green has been instilled in the eye.

Enrollment

30 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • conjunctival staining

Exclusion criteria

  • ocular pathology

Trial design

30 participants in 3 patient groups

2.5 microliters lissamine green
Treatment:
Other: 2.5/5.0/10.0 µL lissamine green
5.0 microliters lissamine green
Treatment:
Other: 2.5/5.0/10.0 µL lissamine green
10.0 microliters lissamine green
Treatment:
Other: 2.5/5.0/10.0 µL lissamine green

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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