Corneal Opacity

3

Review clinical trials related to Corneal Opacity. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Clinical Outcomes of the Gore Synthetic Cornea Device

Study objective is to evaluate the initial safety and effectiveness of the GORE Synthetic Cornea Device in the treatment of loss of corneal clarity in patients who are candidates for corneal transplantation

Participants needed: 10
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: W.L.Gore & AssociatesUpdated: Dec 4, 2025Locations: 2
Eligibility criteria

Patients must meet all of the following criteria to be eligible to be consented... [+10]

Inability to provide written informed consent and comply with study assessments... [+38]

Status: Recruiting

OCT in Diagnosis of Irregular Corneas

This main goal of this study is to improve the detection, classification, monitoring, and treatment of irregular corneas due to keratoconus, warpage, dry eye, scar, stromal dystrophies, and other corneal conditions. The primary goal will be achieved by using optical coherence tomography (OCT) to: 1. Develop an OCT-based system to classify and evaluate corneal-shape irregularities. 2. Develop OCT metrics for more sensitive detection of keratoconus progression. 3. Develop OCT-and-topography guided phototherapeutic keratectomy (PTK) for irregular corneas.

Participants needed: 445
Trial details
Age: 14-85Biological sex: AllType: ObservationalSponsor: Oregon Health and Science UniversityUpdated: Sep 9, 2025Locations: 1
Eligibility criteria

CDVA ≥ 20/25 in the better eye; and both of the following in the worse eye [+17]

Inability to give informed consent. [+5]

Status: Recruiting

Optical Coherence Tomography Guided Transepithelial Phototherapeutic Keratectomy

Optical Coherence Tomography (OCT) machines are non-contact instruments that can measure the depth of scars and other causes of cloudiness in the front of the cornea. The purpose of this study is to determine whether OCT-guided settings for the lasers used for removal of corneal scars and other partial-thickness corneal defects result in improved vision in patients receiving these procedures.

Participants needed: 80
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Oregon Health and Science UniversityUpdated: Feb 12, 2024Locations: 1
Eligibility criteria

Patients with vision primarily limited by superficial opacities and irregulariti...

Inability to give informed consent [+4]