Success Metrics

Clinical Success Rate
100.0%

Based on 5 completed trials

Completion Rate
100%(5/5)
Active Trials
0(0%)
Results Posted
100%(5 trials)

Phase Distribution

Ph not_applicable
5
100%

Phase Distribution

0

Early Stage

0

Mid Stage

0

Late Stage

Phase Distribution5 total trials
N/ANon-phased studies
5(100.0%)

Highest Phase Reached

Unknown

Trial Status & Enrollment

Completion Rate

100.0%

5 of 5 finished

Non-Completion Rate

0.0%

0 ended early

Currently Active

0

trials recruiting

Total Trials

5

all time

Status Distribution
Completed(5)

Detailed Status

Completed5

Development Timeline

Analytics

Development Status

Total Trials
5
Active
0
Success Rate
100.0%
Most Advanced
N/A

Trials by Phase

N/A5 (100.0%)

Trials by Status

completed5100%

Recent Activity

0 active trials
Showing 5 of 5
completednot_applicable

Clinical Evaluation of DAILIES TOTAL 1® Multifocal Compared to 1-Day Acuvue® Moist® Multifocal in a Japanese Population

NCT03341923
completednot_applicable

Assessing Fitting Guides in Alcon Multifocal Contact Lenses

NCT03118934
completednot_applicable

Initial Performance of a Daily Disposable Contact Lens Featuring Molded Marks

NCT02939170
completednot_applicable

Clinical Assessment of DAILIES TOTAL1® (DT1) Multifocal

NCT02871375
completednot_applicable

Evaluation of a New Daily Disposable Multifocal Contact Lens Design

NCT01951573

Clinical Trials (5)

Showing 5 of 5 trials
NCT03341923Not Applicable

Clinical Evaluation of DAILIES TOTAL 1® Multifocal Compared to 1-Day Acuvue® Moist® Multifocal in a Japanese Population

Completed
NCT03118934Not Applicable

Assessing Fitting Guides in Alcon Multifocal Contact Lenses

Completed
NCT02939170Not Applicable

Initial Performance of a Daily Disposable Contact Lens Featuring Molded Marks

Completed
NCT02871375Not Applicable

Clinical Assessment of DAILIES TOTAL1® (DT1) Multifocal

Completed
NCT01951573Not Applicable

Evaluation of a New Daily Disposable Multifocal Contact Lens Design

Completed

All 5 trials loaded

Drug Details

Intervention Type
DEVICE
Total Trials
5