Clinical Outcome of Lipiflow Treatment Prior to Cataract Surgery in Dry Eye Patients
NCT ID: NCT04457999
Last Updated: 2020-07-07
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
100 participants
INTERVENTIONAL
2020-03-20
2020-07-30
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.
Efficacy of Low-Level Light Therapy in Reducing Dry Eye in Patients Undergoing Cataract Surgery
NCT05754437
Stability of Biometry in Meibomian Gland Dysfunction
NCT04322656
High-Definition 3D Visualization System for Ophthalmic Surgery
NCT02194543
Comparison of Clinical Outcomes in Ziemer Femtosecond Versus Conventional Phacoemulsification Surgery
NCT03351894
Clinical Evaluation of Efficacy and Stability of AT TORBI 709M 4-haptic Toric IOL in Cataract Surgery
NCT02618018
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.
Lipiflow treatment
Lipiflow thermal pulsation prior to cataract surgery
Lipiflow Thermal pulsation
Single vectored thermal pulsation treatment for dry eye
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Lipiflow Thermal pulsation
Single vectored thermal pulsation treatment for dry eye
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Patients whose visual acuity anticipated better than 20/25 after surgery
* Patients with informed consent
* Patients with meibomian gland dysfunction
Exclusion Criteria
* uncontrolled systemic disease
* Contact lens wear within 1 month
* Allergic to fluorescein sodium or topical anesthetics
* ocular surgery or trauma within 6 months
* disorder of lid anatomy
* other reason for decreased vision other than cataract
* anticipated visual acuity less than 20/25
* Patients less than 20 years.
21 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Samsung Medical Center
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
tae-young chung
M.D. Ph.D
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Samsung Medical Center
Seoul, , South Korea
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.
2019-03-011
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.