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Clinical Investigation of the TECNIS® Next-Generation Intraocular Lens
Clinical Investigation of the TECNIS® Next-Generation Intraocular Lens
CompletedNA
Sponsor: Johnson & Johnson Surgical Vision, Inc.
Conditions: Cataracts
Interventions: Test IOL Model DEN00V, Control IOL Model DCB00
Countries: United States
Prospective, multicenter, bilateral, interventional, controlled, masked (sponsor, subjects, and evaluators), randomized clinical trial.
Eligibility overview
Sex: ALL
Age: 22 Years to —
Healthy volunteers: Yes
Study type: INTERVENTIONAL
Eligibility criteria
INCLUSION CRITERIA To be considered for enrollment in this study, patient must: * be at least 22 years old * have cataracts in both eyes * sign the written informed consent * be willing and able to comply with examination procedures * understand, read and write English to complete informed consent and questionnaires * be available for study follow-up visits EXCLUSION CRITERIA Patient will not be eligible to take part in the study if: * currently participating in any other clinical study or have participated in a clinical study during the last 30 days * have a certain disease/illness, such as poorly controlled diabetes * have certain ocular conditions, such as uncontrolled pressure in the eye * taking medication that may affect vision * pregnant, plan to become pregnant during the study, or are breastfeeding
Locations (9)
- Bakersfield, California, United States
- Jacksonville, Florida, United States
- Sioux City, Iowa, United States
- Garden City, New York, United States
- Brecksville, Ohio, United States
- Sioux Falls, South Dakota, United States
- Houston, Texas, United States
- Houston, Texas, United States
- San Antonio, Texas, United States