Trials / Unknown
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
| Type | Name | Description |
|---|---|---|
| DRUG | Permethrin 5% | Facial skin application once a night for 3 months. |
| DRUG | Synthomycine 5% | Eye ointment, eyelids and eyelashes application (chloramphenicol), once a night for 3 months. |
| DRUG | Fusidic Acid 1% M/R Eye Drops | viscous 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.