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The effect of betadine in viral eye infection

Comparison of the effect of consumption of 4% betadine and Fluocort eye drops with Fluocort eye drop alone on the duration of the illness of patients with Epidemic keratoconjunctivitis, referred to Nikokary Hospital

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015010920619N1
Enrollment
100
Registered
2015-04-29
Start date
2015-02-20
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Acute adenoviral follicular conjunctivitis. Conjunctivitis due to adenovirus

Interventions

Intervention 1: Intervention 1 (intervention group): For the patients in this group, .4% betadin eye drop will be prescribed with a dosage of one drop every 4 hours daily. 1% Floucort eye drop, will a
Treatment - Drugs
Intervention 1 (intervention group): For the patients in this group, .4% betadin eye drop will be prescribed with a dosage of one drop every 4 hours daily. 1% Floucort eye drop, will also be prescribe
Intervention 2 (control group) : For the patients in this group, 1% foucort eye drop will be prescribed with a dosage of one drop every 6 hours daily ( as a standard medication for this disease). Arti

Sponsors

Vice chancellor for research, Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Viral infection with adenovirus diagnosed with PCR Exclusion criteria: Pregnant women, history of allergy to betadine.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Duration of illness. Timepoint: Before intervention, three days after intervention, one week after intervention, two weeks after intervention,. Method of measurement: The questionnaire.;Pseudomembrane / membrane formation. Timepoint: Before intervention, three days after intervention, seven days after intervention and two weeks after intervention. Method of measurement: Slit lamp examination.

Secondary

MeasureTime frame
Foreign-body sensation in the eye. Timepoint: Before intervention, three days after intervention , one week after intervention, 2 weeks after intervention. Method of measurement: Asking the patients and scaling from zero to 10.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBehzad Fallahi Motlag

Nikokary Hospital

rajchj@gmail.com+98 41 3657 7331

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026