Device
LipiFlow Thermal Pulsation System
LipiFlow Thermal Pulsation System is a medical device with 4 clinical trials. Historical success rate of 100.0%.
Total Trials
4
Max Phase
—
Type
DEVICE
Molecule
—
Success Metrics
Clinical Success Rate
100.0%
Based on 4 completed trials
Completion Rate
100%(4/4)
Active Trials
0(0%)
Results Posted
50%(2 trials)
Phase Distribution
Ph not_applicable
4
100%
Phase Distribution
0
Early Stage
0
Mid Stage
0
Late Stage
Phase Distribution4 total trials
N/ANon-phased studies
4(100.0%)
Highest Phase Reached
UnknownTrial Status & Enrollment
Completion Rate
100.0%
4 of 4 finished
Non-Completion Rate
0.0%
0 ended early
Currently Active
0
trials recruiting
Total Trials
4
all time
Status Distribution
Completed(4)
Detailed Status
Completed4
Development Timeline
Analytics
Development Status
Total Trials
4
Active
0
Success Rate
100.0%
Most Advanced
N/A
Trials by Phase
N/A4 (100.0%)
Trials by Status
completed4100%
Recent Activity
0 active trials
Showing 4 of 4
completednot_applicable
Efficacy of LipiFlow in Patients Affected by Meibomian Gland Dysfunction in Reducing Post-cataract Surgery Dry Eye
NCT05062564
completednot_applicable
Comparison Between iLux and LipiFlow in the Treatment of Meibomian Gland Dysfunction (MGD): A 12-month, Multicenter Study
NCT03956225
completednot_applicable
A Post-Market Evaluation of LipiFlow Treatment in Cataract Surgery Practice
NCT03708367
completednot_applicable
Lipiflow vs iLux Patient Acceptance and Comfort Study
NCT04454983
Clinical Trials (4)
Showing 4 of 4 trials
NCT05062564Not Applicable
Efficacy of LipiFlow in Patients Affected by Meibomian Gland Dysfunction in Reducing Post-cataract Surgery Dry Eye
NCT03956225Not Applicable
Comparison Between iLux and LipiFlow in the Treatment of Meibomian Gland Dysfunction (MGD): A 12-month, Multicenter Study
NCT03708367Not Applicable
A Post-Market Evaluation of LipiFlow Treatment in Cataract Surgery Practice
NCT04454983Not Applicable
Lipiflow vs iLux Patient Acceptance and Comfort Study
All 4 trials loaded
Drug Details
- Intervention Type
- DEVICE
- Total Trials
- 4