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Treatment of Epidemic Keratoconjunctivitis With 2% Povidone-iodine

Treatment of Epidemic Keratoconjunctivitis With 2% Povidone-iodine

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01179412
Enrollment
172
Registered
2010-08-11
Start date
2004-07-31
Completion date
2009-12-31
Last updated
2010-08-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Viral Conjunctivitis

Brief summary

The purpose of this study is to determine the outcomes of treating epidemic keratoconjunctivitis with 2% povidone-iodine.

Detailed description

The study design was a prospective interventional case series. Our institutional ethical committee approved the study protocol in April 2004. We performed this study between July 2004 and December 2009. During this period, there were 2 episodes of EKC epidemic. The first episode was in 2006 and the second in 2009.

Interventions

DRUG2% povidone-iodine

apply 4 times a day for one week

Sponsors

Mahidol University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
7 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patients who were diagnosed with EKC at the outpatient ophthalmic unit

Exclusion criteria

* children younger than six years * women being pregnant or during lactation * history of allergy to povidone-iodine * prior ocular surgery * contact lens usage and chronic eye diseases with current eye medications.

Design outcomes

Primary

MeasureTime frame
the recovery rate within one week of treatment1 week

Secondary

MeasureTime frameDescription
drug tolerability1 weekproportion of patient who can continue topical application of povidone-iodine for a week or until EKC subsides

Countries

Thailand

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026