eurostimulation versus Artificial Tears to Treat Post-LASIK Dry Eye in Adults Measured via Two Dry Eye Questionnaires

Oculeve, Inc.0 个研究点目标入组 60 人开始时间: 2014年3月14日最近更新: 2020年1月13日

试验速览

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•Patients meeting all criteria for appropriateness of LASIK surgery instituted by the treating centre with an established date for bilateral primary LASIK surgery
•Willing to sign the informed consent and deemed capable of complying with the requirements of the study protocol
•Normal lid anatomy, blinking function and closure
•Corrected visual acuity of 20/25 (Snellen equivalent) or better in each eye

•Cardiac demand pacemaker, implanted defibrillator, or other active implanted metallic or electronic device
•Diagnosed epilepsy with seizures within the past five years
•Coagulation disorders such as haemophilia and thrombocytopenia
•Active or uncontrolled severe systemic allergy, chronic seasonal allergies, rhinitis or sinusitis requiring treatment or active/untreated nasal infection at the time of the baseline examination
•Punctal plugs
•Contact lens wear during the study
•Lacrimal, nasal or sinus neoplasia, significant trauma, or invasive surgery
•Chronic or recurrent epistaxis, history of cocaine abuse, or Wegener’s granulomatosis
•Participation in any clinical trial with a new active substance or a new device during the past three months
•Women who are pregnant, planning a pregnancy or nursing at study entry

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