Effect on Wound Healing of Vigamox Versus Cravit
Launched by ALCON RESEARCH · Feb 9, 2009
Trial Information
Current as of May 14, 2025
Completed
Keywords
ClinConnect Summary
No description provided
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Patients of any race and either sex, and over the age of 18, who are scheduled for removal of a cataract and implantation of a posterior chamber intraocular lens using clear corneal incisions or near-clear corneal incisions.
- • Intraocular pressure (IOP) readings, treated or untreated, less than or equal to 20 mmHg prior to surgery. Glaucoma patients are eligible if an ocular hypotensive agent (only one) controls their IOP.
- • Other than cataracts, have normal healthy eyes as determined by the ophthalmic examination and case history.
- • Subconjunctival injections right after cataract surgery are allowed.
- • Other protocol-defined inclusion criteria may apply.
- Exclusion Criteria:
- • Any cataract wound that is stitched or any gross abrasion of the epithelium after removal of a cataract and implantation of a posterior chamber intraocular lens.
- • Fluorescein staining of the cornea at baseline.
- • History or evidence of ocular or systemic disease, which would preclude participation in this study. Examples could include autoimmune disease affecting the cornea as well as any corneal dystrophies.
- • History of ocular inflammatory disease, ocular herpes infection, iritis, uveitis, or Sjögren's syndrome.
- • Known or suspected allergy or hypersensitivity to levofloxacin or any related medicines, such as cinoxacin (Cinobac), ciprofloxacin (Cipro or Ciloxan), norfloxacin (Chibroxin or Noroxin), ofloxacin (Floxin), or nalidixic acid (NegGram), preservatives, dyes, or any components of the study medication.
- • Treatment for an ocular infection within 30 days prior to study entry.
- • Use of topical or systemic steroids within 7 days prior to study entry.
- • Use of topical anti inflammatory drugs within 7 days prior to study entry.
- • Pregnancy, nursing/lactation, or inadequate birth control methods. Oral contraceptives are allowed.
- • Patients with uncontrolled diabetes and/or diabetic retinopathy.
- • No ointment is used after cataract surgery.
- • Other protocol-defined exclusion criteria may apply.
About Alcon Research
Alcon Research is a leading global company dedicated to advancing eye care through innovative research and development. As a subsidiary of Novartis, Alcon focuses on the development of cutting-edge products and therapies for vision correction and eye health, including surgical, pharmaceutical, and consumer eye care solutions. With a commitment to enhancing the quality of life for patients worldwide, Alcon Research conducts rigorous clinical trials to evaluate the safety and efficacy of its products, ensuring that they meet the highest standards of care. Through collaboration with healthcare professionals and institutions, Alcon remains at the forefront of ophthalmic advancements, driving progress in the field of vision science.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Seoul, , Korea, Republic Of
Patients applied
Trial Officials
Eung Kweon Kim, MD/PhD
Principal Investigator
Severance Hospital, Yousei University College of Medicine
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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