Breast cancer Patients' vision under the microscope
NCT ID NCT06767462
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study checks the eye health of people with breast cancer using standard tests like vision charts, eye exams, and scans. The goal is to spot any vision changes or eye damage that might happen during cancer treatment. About 160 participants will be followed to understand how breast cancer and its treatments affect the eyes.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could help doctors monitor and protect vision in breast cancer patients during treatment.
- What could go wrong
- This is an observational safety study, not a treatment trial. It may not lead to direct changes in care.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 160 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2025
- Expected to finish
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Apr 2027
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients who are currently participating in qualifying studies
- Ages
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18 to 130 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Signed informed consent in the qualifying study. 2. Signed informed consent in the ophthalmic study prior to any ophthalmic study specific assessments and procedures. 3. Completed the baseline ophthalmic examination for this study before the first dose in the qualifying study. 4. Meets all the eligibility criteria in the qualifying study Exclusion Criteria: 1. Patients not randomized and not receiving study assigned treatment in a qualifying study. 2. Patients with contraindications to any ophthalmic procedure required by the study or sensitivity/allergy to pupil dilating agents. 3. Judgement by the investigator that the patient should not participate in the ophthalmic study if the patient is unlikely to comply with study procedures, restrictions, and requirements
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Research Site
La Jolla, California, 92093, United States
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Research Site
Palo Alto, California, 94304, United States
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Research Site
Iowa City, Iowa, 52242, United States
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Research Site
Winston-Salem, North Carolina, 27104, United States
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Research Site
Clairton, Pennsylvania, 15025, United States
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Research Site
Pittsburgh, Pennsylvania, 15219, United States
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Research Site
Sioux Falls, South Dakota, 57105, United States
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Research Site
Bartlett, Tennessee, 38133, United States
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Houston, Texas, 77030, United States
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Research Site
CABA, C1061, Argentina
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Research Site
Córdoba, 5008, Argentina
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Research Site
Leuven, 3000, Belgium
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Research Site
Liège, 4000, Belgium
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Research Site
Alfenas, 37130-000, Brazil
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Research Site
Belo Horizonte, 30130-100, Brazil
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Research Site
Curitiba, 80810-050, Brazil
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Research Site
Lajeado, 95900000, Brazil
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Research Site
Porto Alegre, 90050-170, Brazil
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Research Site
Pouso Alegre, 37554-216, Brazil
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Research Site
São Paulo, 01321-001, Brazil
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Research Site
Sorocaba, 18060-105, Brazil
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Research Site
Três Lagoas, 79601-001, Brazil
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Research Site
Vitória, 29055-450, Brazil
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Research Site
Montreal, Quebec, H2X 3E4, Canada
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Research Site
Montreal, Quebec, H4A 3J1, Canada
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Research Site
Santiago, 7500587, Chile
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Research Site
Santiago, 7620157, Chile
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Research Site
Ashdod, 7747629, Israel
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Research Site
Nahariya, 2210001, Israel
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Research Site
Lodz, 90-302, Poland
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Research Site
Amadora, 2720-276, Portugal
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Research Site
Braga, 4710-243, Portugal
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Research Site
Seoul, 6351, South Korea
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Research Site
Badalona, 08003, Spain
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Research Site
Barcelona, 08028, Spain
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Research Site
Barcelona, 08035, Spain
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Research Site
Barcelona, 08036, Spain
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Research Site
Girona, 17007, Spain
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Research Site
L'Hospitalet de Llobregat, 08908, Spain
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Research Site
Leganés, 28911, Spain
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Research Site
Madrid, 28007, Spain
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Research Site
Madrid, 28009, Spain
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Research Site
Madrid, 28033, Spain
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Research Site
Madrid, 28034, Spain
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Research Site
Madrid, 28040, Spain
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Research Site
Madrid, 28041, Spain
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Research Site
Madrid, 28050, Spain
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Research Site
Majadahonda, 28222, Spain
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Research Site
Salamanca, 37007, Spain
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Research Site
Sant Joan Despí, 08970, Spain
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Other studies related to the condition(s) this trial covers.
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- Can a common steroid shield breast cancer patients from a dangerous drug side effect?