A Safety and Effectiveness Study of PRK Using the ALLEGRETTO WAVE® EYE-Q Excimer Laser System
Not Applicable
Completed
- Conditions
- AstigmatismMyopia
- Interventions
- Procedure: Photorefractive keratectomy (PRK)Device: ALLEGRETTO WAVE EYE-Q excimer laser system
- First Posted Date
- 2012-10-03
- Last Posted Date
- 2019-09-30
- Lead Sponsor
- Alcon Research
- Target Recruit Count
- 176
- Registration Number
- NCT01699087
A Six-Week Safety Study of an Investigational Ophthalmic Solution
Phase 3
Completed
- Conditions
- Allergic Conjunctivitis
- Interventions
- Drug: AL-4943A Ophthalmic SolutionDrug: AL-4943A Ophthalmic Solution Vehicle
- First Posted Date
- 2012-10-03
- Last Posted Date
- 2014-03-27
- Lead Sponsor
- Alcon Research
- Target Recruit Count
- 518
- Registration Number
- NCT01698814
Confocal Analysis of Corneal Structures of Symptomatic Allergic Conjunctivitis Patients
Phase 4
Completed
- Conditions
- Allergic Conjunctivitis
- Interventions
- First Posted Date
- 2012-10-02
- Last Posted Date
- 2014-08-18
- Lead Sponsor
- Alcon Research
- Target Recruit Count
- 17
- Registration Number
- NCT01697969
- Locations
- 🇺🇸
University of Iowa, Iowa City, Iowa, United States
Assessing the Efficacy of DuoTrav as a Replacement Therapy in Glaucoma Patients in Russia
Phase 4
Withdrawn
- Conditions
- GlaucomaOcular Hypertension
- Interventions
- First Posted Date
- 2012-10-01
- Last Posted Date
- 2013-02-07
- Lead Sponsor
- Alcon Research
- Registration Number
- NCT01696383
Evaluation of SYSTANE® BALANCE in Dry Eye Subjects With Lipid Deficiency
Not Applicable
Completed
- Conditions
- Dry Eye SyndromeLipid Deficiency
- Interventions
- Other: SYSTANE® BALANCE eyedropsOther: Minims® Saline 0.9% eyedrops
- First Posted Date
- 2012-09-20
- Last Posted Date
- 2018-06-29
- Lead Sponsor
- Alcon Research
- Target Recruit Count
- 91
- Registration Number
- NCT01688726
Evaluation of the Effectiveness of Two Marketed Multi-Purpose Solutions for Silicone Hydrogel Contact Lenses - Study 2
Not Applicable
Completed
- Conditions
- MyopiaContact Lens ComfortHyperopia
- Interventions
- Device: Opti-Free® PureMoist® MPDSDevice: RevitaLens MPDSDevice: Habitual Contact Lenses
- First Posted Date
- 2012-09-12
- Last Posted Date
- 2014-04-29
- Lead Sponsor
- Alcon Research
- Target Recruit Count
- 196
- Registration Number
- NCT01684046
Evaluation of the Effectiveness of Two Marketed Multi-Purpose Solutions for Silicone Hydrogel Contact Lenses - Study 1
Not Applicable
Completed
- Conditions
- HyperopiaContact Lens ComfortMyopia
- Interventions
- Device: Opti-Free® PureMoist® MPDSDevice: Biotrue™ MPSDevice: Habitual contact lenses
- First Posted Date
- 2012-09-12
- Last Posted Date
- 2014-04-17
- Lead Sponsor
- Alcon Research
- Target Recruit Count
- 207
- Registration Number
- NCT01684033
A Clinical Outcome Study of Two Multifocal Intraocular Lenses (IOL) in Cataract Patients
Not Applicable
Completed
- Conditions
- Cataracts
- Interventions
- Device: AcrySof® IQ ReSTOR® +2.5 D Multifocal IOL Model SN6AD2 [SV25T0]Device: AcrySof® IQ ReSTOR® +3.0 D Multifocal IOL Model SN6AD1
- First Posted Date
- 2012-09-12
- Last Posted Date
- 2015-06-22
- Lead Sponsor
- Alcon Research
- Target Recruit Count
- 112
- Registration Number
- NCT01684007
An Efficacy and Tolerability Study of TRAVATAN® Versus LUMIGAN®
Phase 4
Completed
- Conditions
- GlaucomaOcular Hypertension
- Interventions
- First Posted Date
- 2012-08-14
- Last Posted Date
- 2015-08-03
- Lead Sponsor
- Alcon Research
- Target Recruit Count
- 104
- Registration Number
- NCT01664039
Pharmacokinetic and Safety Study of Travoprost 0.004% in Pediatric Glaucoma Patients
Phase 1
Completed
- Conditions
- GlaucomaOcular Hypertension
- Interventions
- First Posted Date
- 2012-08-07
- Last Posted Date
- 2016-04-01
- Lead Sponsor
- Alcon Research
- Target Recruit Count
- 25
- Registration Number
- NCT01658839
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