Device
DisCoVisc
DisCoVisc 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 5 completed trials
Completion Rate
100%(5/5)
Active Trials
0(0%)
Results Posted
80%(4 trials)
Phase Distribution
Ph phase_3
1
20%
Ph phase_4
3
60%
Ph not_applicable
1
20%
Phase Distribution
0
Early Stage
0
Mid Stage
4
Late Stage
Phase Distribution5 total trials
Phase 3Large-scale testing
1(20.0%)
Phase 4Post-market surveillance
3(60.0%)
N/ANon-phased studies
1(20.0%)
Highest Phase Reached
Phase 4Trial 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
Phase 4
Trials by Phase
Phase 31 (20.0%)
Phase 43 (60.0%)
N/A1 (20.0%)
Trials by Status
completed5100%
Recent Activity
0 active trials
Showing 5 of 5
completednot_applicable
Influence of DisCoVisc Ophthalmic Viscosurgical Device (OVD) on Intraoperative Aberrometry Readings
NCT03751033
completedphase_4
To Compare the Ability of DiscoVisc® OVD to Protect the Corneal Endothelium and Maintain Anterior Chamber Space With Healon® and Amvisc® PLUS During Cataract Surgery.
NCT00763360
completedphase_4
DisCoVisc Versus DuoVisc, Healon5 and AmVisc Plus
NCT00712244
completedphase_4
Intraoperative Floppy Iris Syndrome
NCT00711347
completedphase_3
DisCoVisc Comparative Evaluation
NCT00732225
Clinical Trials (5)
Showing 5 of 5 trials
NCT03751033Not Applicable
Influence of DisCoVisc Ophthalmic Viscosurgical Device (OVD) on Intraoperative Aberrometry Readings
NCT00763360Phase 4
To Compare the Ability of DiscoVisc® OVD to Protect the Corneal Endothelium and Maintain Anterior Chamber Space With Healon® and Amvisc® PLUS During Cataract Surgery.
NCT00712244Phase 4
DisCoVisc Versus DuoVisc, Healon5 and AmVisc Plus
NCT00711347Phase 4
Intraoperative Floppy Iris Syndrome
NCT00732225Phase 3
DisCoVisc Comparative Evaluation
All 5 trials loaded
Drug Details
- Intervention Type
- DEVICE
- Total Trials
- 5