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The Efficacy of Permethrin 5%, Fusidic Acid 1% and Synthomycine 5% for Demodex - Blepharitis

The Efficacy Of Lyclear (Permethrin 5%) Vs Fusidic Acid1% and Synthomycine 5% for Demodex -Blepharitis Treatment, Prospective-Randomized Trial.

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03105505
Enrollment
75
Registered
2017-04-10
Start date
2017-04-28
Completion date
2018-09-30
Last updated
2018-01-30

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

Conditions

Inflammation of the Eyelids

Brief summary

The study aims to investigate the effect of Permethrin 5% treatment on Signs and symptoms of Demodex-blepharitis in comparison to Synthomycine 5% and Fucithalmic (fusidic acid 1%) .

Detailed description

3 arms study. 75 patient total, 25 patients in each group. Group A (study group) patients will apply facially Permethrin 5% every night for 3 months. Group B patients will apply on the eyelids Fusidic acid 1% every night for 3 months. Group C patients will apply on the eyelids Synthomycine 5% every night for 3 months Follow up Evaluation will be made after one week, one month, two months, three months, 4 months and half a year.

Interventions

Facial skin application once a night for 3 months.

DRUGSynthomycine 5%

Eye ointment, eyelids and eyelashes application (chloramphenicol), once a night for 3 months.

DRUGFusidic Acid 1% M/R Eye Drops

viscous eye drops application once a night for 3 months.

Sponsors

Barzilai Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

\- Adult (Age ≥18Y) individuals clinically diagnosed with Demodex- blepharitis.

Exclusion criteria

\- Known sensitivity to all study medications or components. Pregnant women and individuals deemed unfit to provide informed consent. Systemic steroid use.

Design outcomes

Primary

MeasureTime frameDescription
Decrease in demodex infestation in group A (permethrin 5%).2 monthssignificant decrease in demodex infestation in comparison to group B and C.
Improvement in symptoms and complaints in group A.2 monthsOSDI Questionnaires that describe the severity of the ocular surface disease condition are filled in each visit.

Countries

Israel

Outcome results

None listed

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