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UnknownNCT03105505

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
Phase
Phase 4
Study type
Interventional
Enrollment
75 (estimated)
Sponsor
Barzilai Medical Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGPermethrin 5%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 Dropsviscous eye drops application once a night for 3 months.

Timeline

Start date
2017-04-28
Primary completion
2018-09-01
Completion
2018-09-01
First posted
2017-04-10
Last updated
2018-01-30

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT03105505. Inclusion in this directory is not an endorsement.