Tea Tree Oil in the Treatment of Chronic Blepharitis
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|ClinicalTrials.gov Identifier: NCT01073150|
Recruitment Status : Completed
First Posted : February 23, 2010
Last Update Posted : February 23, 2010
The purpose of this study is to determine:
- The prevalence of Demodex sp. in chronic blepharitis.
- The efficacy of the treatment of topical Tree Tea Oil in chronic blepharitis for Demodex sp.
|Condition or disease||Intervention/treatment||Phase|
|Blepharitis||Drug: Tea Tree Oil||Phase 2|
Patients with clinical diagnosis of chronic blepharitis were included in this study. A check list of symptoms and an ophthalmologic examination including best corrected visual acuity and biomicroscopy were performed.
Under a slit lamp visualization, three lashes with cylindrical dandruff of each eyelid were epilated by fine forceps. The lashes were immersed in fluorescein dye and examined under a light microscope at a 20-times magnification. The mites were detected based on its morphological characteristics and movement.
The patients with chronic blepharitis who had Demodex were randomly divided in two groups. The treatment group was prescribed lid hygiene with Tea Tree Oil shampoo 0.25% and ointment 5% daily and Tea Tree Oil oily solution 50% once a week - produced by Ophthalmos, São Paulo. The control group used the same posology of placebo similar products.
After six weeks, all subjects underwent the initial clinical and laboratory examination. The symptoms and the quantity of mites (mites/eye) were compared before and after the treatment in both groups.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||34 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Double (Participant, Investigator)|
|Official Title:||Tea Tree Oil in the Treatment of Chronic Blepharitis|
|Study Start Date :||April 2009|
|Actual Primary Completion Date :||August 2009|
|Actual Study Completion Date :||November 2009|
- Drug: Tea Tree Oil
Tea Tree Oil shampoo 0.25% and ointment 5% daily and Tea Tree Oil oily solution 50% once a week for six weeks
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01073150
|Federal University of Sao Paulo|
|Sao Paulo, SP, Brazil, 04038040|
|Principal Investigator:||Nahin Geha||Federal University of São Paulo|