1. Comparison of the clinical efficacy of preserved and preservative-free hydroxypropyl methylcellulose-dextran-containing eyedrops
- Author
-
Pedram Akbarshahi, Parvin Azizzadeh, and Masoud Safarzadeh
- Subjects
Male ,0301 basic medicine ,Preservative ,medicine.medical_treatment ,Artificial tear drops ,Administration, Ophthalmic ,Cornea ,chemistry.chemical_compound ,Benzalkonium chloride ,Hypromellose Derivatives ,0302 clinical medicine ,lcsh:Ophthalmology ,Surveys and Questionnaires ,lcsh:QC350-467 ,Single-Blind Method ,Ocular Surface Disease Index ,Clinical efficacy ,Hydroxypropyl methylcellulose ,Dextrans ,Middle Aged ,Drug Combinations ,Artificial tears ,Treatment Outcome ,Dextran ,Original Article ,Dry Eye Syndromes ,Female ,Benzalkonium Compounds ,lcsh:Optics. Light ,medicine.drug ,Adult ,Lágrimas artificiales ,medicine.medical_specialty ,Hidroxipropil metilcelulosa ,Lubricant Eye Drops ,03 medical and health sciences ,Ophthalmology ,medicine ,Humans ,Dry eye syndrome ,business.industry ,Preservatives, Pharmaceutical ,Eyelids ,Repeated measures design ,Síndrome de ojo seco ,Dextran 70 ,030104 developmental biology ,chemistry ,lcsh:RE1-994 ,Tears ,030221 ophthalmology & optometry ,Ophthalmic Solutions ,business ,Optometry - Abstract
Purpose: This study aimed to compare the efficacy of two sustained-release formulation of artificial tear drops. Patients and methods: This is a randomized patient-masked clinical trial, a total 88 patients into two group A (n = 41; with single dose of artificial tear, containing dextran 70, 1 mg/ml and hypromellose, 3 mg/ml hydroxypropyl methylcellulose (HPMC) and group B (n = 47; with multidose of artificial tear, containing 0.3 g HPMC and 0.1 g of dextran 70, with 0.01% benzalkonium chloride (BAK) as preservative) were completed the study. The ocular surface disease index (OSDI) questionnaire, tear break up time (TBUT), corneal and conjunctival staining and Schirmer test, were performed. Repeated measures ANOVA was used to assess the differences among the two products. A p-value less than 0.05 was considered significant. Results: The mean of age of the participants in the Group A and B was 44.08 ± 6.29 (range, 33–58 years) years and 45.83 ± 8.42 (31–60 years), respectively. In comparing two groups before the intervention, the OSDI scores, the TBUT scores, the conjunctival and corneal staining scores and the Schirmer scores did not show statistically significant differences (p = 0.339, p = 0.640, p = 0.334, p = 0.807 and p = 0.676, respectively). After 4 weeks, the OSDI scores, conjunctival and corneal staining scores showed improvement in compare to those before the intervention (p
- Published
- 2017
- Full Text
- View/download PDF