Efficacy and safety of diquafosol ophthalmic solution in patients with dry eye syndrome: A Japanese phase 2 clinical trial

Ophthalmology

Volumn 119, Issue 10, 2012, Pages 1954-1960

  Matsumoto, Yukihiro ^a   Ohashi, Yuichi ^b   Watanabe, Hitoshi ^c   Tsubota, Kazuo ^a  

^a KEIO UNIVERSITY   (Japan)

^b EHIME UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c KANSAI ROSAI HOSPITAL   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

DIQUAFOSOL; FLUORESCEIN; PLACEBO; ROSE BENGAL;

ADULT; ARTICLE; BLOOD SAMPLING; BREAK UP TIME; CONJUNCTIVA; CONJUNCTIVAL HYPEREMIA; CONTROLLED STUDY; CORNEA; DOSE RESPONSE; DOUBLE BLIND PROCEDURE; DRUG EFFICACY; DRUG SAFETY; DRY EYE; EYE DISCHARGE; EYE IRRITATION; EYE PAIN; FEMALE; FOREIGN BODY REACTION; HUMAN; JAPANESE; MAJOR CLINICAL STUDY; MALE; MULTICENTER STUDY; PHASE 2 CLINICAL TRIAL; PRIORITY JOURNAL; RANDOMIZED CONTROLLED TRIAL; RATING SCALE; SCORING SYSTEM; SENSATION; SIDE EFFECT; STAINING; TIME; URINALYSIS;

ADMINISTRATION, TOPICAL; CORNEA; DOUBLE-BLIND METHOD; DRY EYE SYNDROMES; FEMALE; FLUOROPHOTOMETRY; HUMANS; JAPAN; MALE; MIDDLE AGED; OPHTHALMIC SOLUTIONS; POLYPHOSPHATES; PROSPECTIVE STUDIES; PURINERGIC P2Y RECEPTOR AGONISTS; TEARS; TREATMENT OUTCOME; URACIL NUCLEOTIDES;

EID: 84867102487     PISSN: 01616420     EISSN: 15494713     Source Type: Journal    
DOI: 10.1016/j.ophtha.2012.04.010     Document Type: Article

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