Clinical Trials Logo
  1. Home
  2. Dry Eye
  3. NCT04457999
  4. Details
NCT04457999 Clinical Trial

Clinical Outcome of Lipiflow Treatment Prior to Cataract Surgery in Dry Eye Patients

Dry Eye Clinical Trial

Official title:
Clinical Outcome of Lipiflow Treatment Prior to Cataract Surgery in Dry Eye Patients

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04457999
Other study ID # 2019-03-011
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 20, 2020
Est. completion date July 30, 2020

Study information
Verified date July 2020
Source Samsung Medical Center
Contact Tae-Young Chung, MD. PhD
Phone 82-2-3410-3563
Email tychung@skku.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To investigate the clinical outcome of Lipiflow treatment prior to cataract surgery in patients with meibomian gland dysfunction and dry eye disease

Recruitment information / eligibility
Status Recruiting
Enrollment 100
Est. completion date July 30, 2020
Est. primary completion date July 2, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years and older
Eligibility Inclusion Criteria:

- Patients older than 21, who will get catarct surgeyr

- Patients whose visual acuity anticipated better than 20/25 after surgery

- Patients with informed consent

- Patients with meibomian gland dysfunction

Exclusion Criteria:

- ocular injury, active injection

- 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.

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Lipiflow Thermal pulsation
Single vectored thermal pulsation treatment for dry eye

Locations
Country Name City State
Korea, Republic of Samsung Medical Center Seoul

Sponsors (1)
Lead Sponsor Collaborator
Samsung Medical Center

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary improvement of dry eye symptom ocular dryness 1 month
See also
  Status Clinical Trial Phase
Completed NCT05027087 - The Effect of a Novel Blueberry Supplement on Dry Eye Disease Phase 3
Completed NCT05102409 - An Exploratory Clinical Trial to Assess Safety and Tolerability in Subjects With Dry Eye Disease Phase 2
Completed NCT06159569 - Performance and Tolerability of the Medical Device LACRIACT N/A
Completed NCT04081610 - Clinical Trial to Evaluate the Safety and Tolerability of Lagricel® Ofteno Multi-dose Ophthalmic Solution Phase 1
Completed NCT05062564 - Efficacy of LipiFlow in Patients Affected by Meibomian Gland Dysfunction in Reducing Post-cataract Surgery Dry Eye N/A
Completed NCT05825599 - PMCF Study to Evaluate Performance and Safety of "HPMC-based Eyedrops" Used to Relieve Dry Eye Symptoms N/A
Completed NCT03418727 - Dry Eye Disease Study With Brimonidine Phase 2
Active, not recruiting NCT04425551 - Effect of Micropulse Laser on Dry Eye Disease Due to Meibomian Gland Dysfunction N/A
Recruiting NCT04527887 - Intracanalicular Dexamethasone Insert for the Treatment of Inflammation and Discomfort in Dry Eye Disease (DEcIDED) Phase 4
Not yet recruiting NCT06379685 - Study to Evaluate the Safety and Tolerability of PRO-190 Ophthalmic Solution Compared to Systane Ultra® on the Ocular Surface. Phase 1
Active, not recruiting NCT05618730 - Safety, Tolerability, Plug Retention and Preliminary Efficacy of Tacrolimus-loaded Punctal Plug in Patients With Moderate to Severe Dry Eye Disease - Cohort B Phase 1
Completed NCT04553432 - Dry Eye OmniLenz Application of Omnigen Research Study Phase 4
Recruiting NCT04109170 - Dry Eye Evaluation System Based on Bioinformatics
Completed NCT04105842 - Refitting Daily Disposable Contact Lens Wearers With Dry Eye Disease With A Different Daily Disposable Lens Type N/A
Completed NCT05505292 - Lifitegrast 5% for the Treatment of Dry Eye In Habitual Soft Contact Lens Wearers Phase 4
Completed NCT04668131 - Study on Curative Effect and Mechanism of Acupuncture on Neuropathic Pain in Dry Eye Disease N/A
Completed NCT06176651 - Evaluation of Miebo (Perfluorohexyloctane) Eyedrops in Habitual Contact Lens Wearers Phase 4
Completed NCT02235259 - Efficacy and Safety of XG-104 for the Treatment of Dry Eye Phase 2
Not yet recruiting NCT02218827 - Topical Steroid Treatment For Dry Eye N/A
Completed NCT01959854 - Efficacy of Topical 0.2% Xanthan Gum in Patients With Dry Eye N/A