Success Metrics

Clinical Success Rate
100.0%

Based on 11 completed trials

Completion Rate
100%(11/11)
Active Trials
0(0%)
Results Posted
45%(5 trials)

Phase Distribution

Ph not_applicable
13
93%

Phase Distribution

0

Early Stage

0

Mid Stage

0

Late Stage

Phase Distribution13 total trials
N/ANon-phased studies
13(100.0%)

Highest Phase Reached

Unknown

Trial Status & Enrollment

Completion Rate

100.0%

11 of 11 finished

Non-Completion Rate

0.0%

0 ended early

Currently Active

0

trials recruiting

Total Trials

14

all time

Status Distribution
Active(1)
Completed(11)
Other(2)

Detailed Status

Completed11
unknown2
Not yet recruiting1

Development Timeline

Analytics

Development Status

Total Trials
14
Active
0
Success Rate
100.0%
Most Advanced
N/A

Trials by Phase

N/A13 (100.0%)

Trials by Status

unknown214%
not_yet_recruiting17%
completed1179%

Recent Activity

Clinical Trials (14)

Showing 14 of 14 trials
NCT02890160Not Applicable

A Trial of Firesorb in Patients With Coronary Artery Disease: FUTURE-II

Completed
NCT07230847Not Applicable

A Study Evaluating the Vascular Healing and Neointimal Transformation at 1 Month After Implantation of BioFreedom™ Drug-coated Stents and the Xience Drug-eluting Stent System in Patients With Acute Coronary Syndrome and High Bleeding Risk Using Optical Coherence Tomography

Not Yet Recruiting
NCT03440801Not Applicable

A Randomized Comparison of Long-Term Healing Between Biodegradable- Versus Durable-Polymer Everolimus Eluting Stents in STEMI

Completed
NCT02173379Not Applicable

Absorb IV Randomized Controlled Trial

Completed
NCT01751906Not Applicable

ABSORB III Randomized Controlled Trial (RCT)

Completed
NCT03815175Not Applicable

XIENCE 28 USA Study

Completed
NCT03218787Not Applicable

XIENCE 90: A Safety Evaluation of 3-month DAPT After XIENCE Implantation for HBR Patients.

Completed
NCT03355742Not Applicable

XIENCE 28 Global Study

Completed
NCT02870140Not Applicable

Thin Strut Sirolimus-eluting Stent in All Comers Population vs Everolimus-eluting Stent

Completed
NCT02579031Not Applicable

A Comparison of an Ultrathin Strut Biodegradable Polymer Sirolimus-Eluting Stent With a Durable Polymer Everolimus-Eluting Stent for Patients With Acute ST-Segment Elevation Myocardial Infarction Undergoing Primary Percutaneous Coronary Intervention

Completed
NCT03049657Not Applicable

Efficacy of Angiolite Stent vs a Second-generation Drug-eluting Stent Xience for Percutaneous Coronary Intervention

Completed
NCT01858077Not Applicable

Amsterdam Investigator-initiateD Absorb Strategy All-comers Trial

Unknown
NCT02486068Not Applicable

ABSORB Bioresorbable Scaffold vs. Xience Metallic Stent for Prevention of Restenosis in Patients at High Risk of Restenosis

Unknown
NCT01350869

Evaluation of Everolimus-Eluting Stents (The K-XIENCE Registry)

Completed

All 14 trials loaded

Drug Details

Intervention Type
DEVICE
Total Trials
14