This study is a comparison of the bioavailability of nutrients contained in softgel capsules
: ICAPS Eye Vitamin and Mineral Supplement - Softgel (full strength)
: ICAPS Eye Vitamin and Mineral Supplement - Softgel (half strength)
: ICAPS Eye Vitamin and Mineral Supplement - Coated Tablets (full strength)
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Locations near you
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Full eligibility criteria for NCT01057966
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Age 18 to 35
Body Mass Index (BMI) 21-27 kg/m2
Must be able to give written informed consent
Subjects must be willing to comply with all study requirements.
Subjects must understand, sign and be given a copy of the written Informed Consent form.
Subjects for whom both eyes do not meet all inclusion criteria and either eye meets exclusion criteria
Subjects who are pregnant, lactating or planning to be pregnant during the course of the study
Subjects with known sensitivity to planned study concomitant medications
Subjects participating in any other ophthalmic drug or device clinical trial within 30 days of this clinical investigation.
Use of ocular drugs, other than study medications, during the study and within 14 days prior to study entry or any other ocular medication
All locations for NCT01057966
United States (1)
Contact Alcon Call Center For Trial Locations
Fort Worth, Texas, United States, 76134
View full eligibility
Tris trial is registered with FDA with number: NCT01057966. The sponsor of the trial is Alcon Research and it is looking for 15 volunteers for the current phase.
Official trial title:
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