Device
Single Vision Contact Lens
Single Vision Contact Lens is a medical device with 5 clinical trials. Historical success rate of 100.0%.
Total Trials
5
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 phase_2
1
20%
Ph not_applicable
3
60%
Phase Distribution
0
Early Stage
1
Mid Stage
0
Late Stage
Phase Distribution4 total trials
Phase 2Efficacy & side effects
1(25.0%)
N/ANon-phased studies
3(75.0%)
Highest Phase Reached
Phase 2Trial 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
5
all time
Status Distribution
Active(1)
Completed(4)
Detailed Status
Completed4
Not yet recruiting1
Development Timeline
Analytics
Development Status
Total Trials
5
Active
0
Success Rate
100.0%
Most Advanced
Phase 2
Trials by Phase
Phase 21 (25.0%)
N/A3 (75.0%)
Trials by Status
not_yet_recruiting120%
completed480%
Recent Activity
0 active trials
Showing 5 of 5
not_yet_recruitingphase_2
Evaluating the Efficacy of the Combination of Multi-zonal Contact Lens and Atropine for Controlling Myopia Progression
NCT06765603
completednot_applicable
Evaluating Contact Lens Optics
NCT05028790
completednot_applicable
Contact Lens Optics and Visual Performance
NCT05308069
completednot_applicable
Accommodative Relief for Uncomfortable Non-Presbyopes
NCT03544216
completed
Evaluation of Visual Performance With Contact Lenses
NCT03705130
Clinical Trials (5)
Showing 5 of 5 trials
NCT06765603Phase 2
Evaluating the Efficacy of the Combination of Multi-zonal Contact Lens and Atropine for Controlling Myopia Progression
NCT05028790Not Applicable
Evaluating Contact Lens Optics
NCT05308069Not Applicable
Contact Lens Optics and Visual Performance
NCT03544216Not Applicable
Accommodative Relief for Uncomfortable Non-Presbyopes
NCT03705130
Evaluation of Visual Performance With Contact Lenses
All 5 trials loaded
Drug Details
- Intervention Type
- DEVICE
- Total Trials
- 5