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Amniotic Fluid (AFED) for Photorefractive Keratectomy
Phase 1 & 2
Waitlist Available
Research Sponsored by University of Utah
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up post-operative months 1, 3, 6, and 12
Awards & highlights
Study Summary
This trial is testing if a new eye drop is safe for people who have a type of eye surgery.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ post-operative months 1, 3, 6, and 12
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~post-operative months 1, 3, 6, and 12
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Safety - Adverse Events Including Serious Adverse Events
Secondary outcome measures
Corneal Staining in Each Eye
Corneal Surface Regularity
Count of Participants Who Reported Oral Pain Medication Usage
+3 moreTrial Design
2Treatment groups
Active Control
Placebo Group
Group I: Amniotic Fluid (AFED)Active Control1 Intervention
Group II: Saline SolutionPlacebo Group1 Intervention
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Who is running the clinical trial?
University of UtahLead Sponsor
1,099 Previous Clinical Trials
1,778,628 Total Patients Enrolled
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Are there any available slots within this research project for participants?
"As per the details posted on clinicaltrials.gov, this specific medical trial is no longer seeking participants; its first posting was on July 10th 2020 and its last update occurred on February 7th 2022. However, two other trials are enrolling patients currently."
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