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Topical Treatment of Bacterial Conjunctivitis and Its Effect on Microbial Flora

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Alcon

Status and phase

Completed
Phase 4

Conditions

Bacterial Conjunctivitis

Treatments

Drug: VIGAMOX

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT00312338
CMS-05-11

Details and patient eligibility

About

Topical Treatment of Bacterial Conjunctivitis and its Effect on Microbial Flora

Enrollment

137 patients

Sex

All

Ages

1 to 13 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients from 1 to 13 years of age that have diagnosis of bacterial conjunctivitis in either or both eyes (for < 3 days duration) based on clinical observation; matched healthy controls

Exclusion criteria

  • Cannot have had bacterial conjunctivitis symptoms as reported by parent for > 2 days

Trial design

137 participants in 2 patient groups

Infected Patient treated with Vigamox
Experimental group
Description:
Conjunctivitis-Infected Patient receiving Vigamox 0.5% in both eyes three times daily for 7 days.
Treatment:
Drug: VIGAMOX
Healthy Subjects
No Intervention group
Description:
Healthy Subjects receiving no treatment

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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