Safety and Efficacy Study BRIMOCHOL™ PF and Carbachol PF in Subjects With Emmetropic Phakic or Pseudophakic Presbyopia
NCT ID: NCT05270863
Last Updated: 2024-10-15
Study Results
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View full resultsBasic Information
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COMPLETED
PHASE3
182 participants
INTERVENTIONAL
2022-03-30
2023-04-10
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
TREATMENT
DOUBLE
Study Groups
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BRIMOCHOL™ PF
A single drop in each eye at a visit.
BRIMOCHOL™ PF
A single drop in each eye at a visit.
Carbachol PF
A single drop in each eye at a visit.
Carbachol PF
A single drop in each eye at a visit.
Brimonidine tartrate
A single drop in each eye at a visit.
Brimonidine tartrate
A single drop in each eye at a visit.
Interventions
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BRIMOCHOL™ PF
A single drop in each eye at a visit.
Carbachol PF
A single drop in each eye at a visit.
Brimonidine tartrate
A single drop in each eye at a visit.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Must have presbyopia
Exclusion Criteria
* Any disease or medical condition that, in the opinion of the Investigator, would prevent the subject from participating in the study or might confound study results
45 Years
80 Years
ALL
Yes
Sponsors
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Visus Therapeutics
OTHER
Responsible Party
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Locations
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Visus Therapeutics Investigative Site
Glendale, California, United States
Visus Therapeutics Investigative Site
Rancho Cordova, California, United States
Visus Therapeutics Investigative Site
Jacksonville, Florida, United States
Visus Therapeutics Investigative Site
Morrow, Georgia, United States
Visus Therapeutics Investigative Site
Roswell, Georgia, United States
Visus Therapeutics Investigative Site
Shawnee Mission, Kansas, United States
Visus Therapeutics Investigative Site
Kansas City, Missouri, United States
Visus Therapeutics Investigative Site
Kansas City, Missouri, United States
Visus Therapeutics Investigative Site
Pittsburgh, Pennsylvania, United States
Visus Therapeutics Investigative Site
Memphis, Tennessee, United States
Visus Therapeutics Investigative Site
Memphis, Tennessee, United States
Visus Therapeutics Investigative Site
Cedar Park, Texas, United States
Visus Therapeutics Investigative Site
Houston, Texas, United States
Visus Therapeutics Investigative Site
San Antonio, Texas, United States
Visus Therapeutics Investigative Site
Ogden, Utah, United States
Countries
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Provided Documents
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Document Type: Study Protocol
Document Type: Statistical Analysis Plan
Other Identifiers
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VT-002
Identifier Type: -
Identifier Source: org_study_id
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