Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
NA
30 participants
INTERVENTIONAL
2009-02-28
2009-08-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Long Term Effects of Multifocal Orthokeratology on Corneal and Choroidal Structures in Healthy Subjects With Myopia- A Pilot Study
NCT02700295
Efficacy of Corneal Cross-Linking (CXL) in the Treatment of Pediatric Keratoconus
NCT07080983
Dry Eye Evaluation After Transepithelial PRK
NCT02210793
Custom Anterior Surfacing of Scleral Lens for Vision Quality Improvement in Patients With Keratoconus
NCT03647046
Monthly Replacement Orthokeratology for Myopia Control in Existing Lens Wearers
NCT04295707
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Keratoconus
One eye of Keratoconus patient
Orthokeratology contact lenses
Wearing Orthokeratology lens in one eye of a keratoconus patient
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Orthokeratology contact lenses
Wearing Orthokeratology lens in one eye of a keratoconus patient
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* No apical scars
Exclusion Criteria
* Apical scaring
* Contact lens intolerance
18 Years
45 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Hadassah Medical Organization
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
: Hadassah Medical Organization, Jerusalem, Israel
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
: Hadassah Medical Organization,
Jerusalem, , Israel
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
dvleyes-HMO-CTIL
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.