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
6
100%

Phase Distribution

0

Early Stage

0

Mid Stage

0

Late Stage

Phase Distribution6 total trials
N/ANon-phased studies
6(100.0%)

Highest Phase Reached

Unknown

Trial 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

6

all time

Status Distribution
Active(1)
Completed(4)
Other(1)

Detailed Status

Completed4
Suspended1
Enrolling by invitation1

Development Timeline

Analytics

Development Status

Total Trials
6
Active
0
Success Rate
100.0%
Most Advanced
N/A

Trials by Phase

N/A6 (100.0%)

Trials by Status

suspended117%
completed467%
enrolling_by_invitation117%

Recent Activity

0 active trials
Showing 5 of 6
suspendednot_applicable

A Pilot Study to Evaluate PureWick for Nocturia

NCT05090722
enrolling_by_invitationnot_applicable

An Evaluation of the PureWick™ Male External Catheter Versus an Established Comparator Overnight in the Home Setting for Incontinence in Adult Males

NCT07282860
completednot_applicable

PureWick™ Adolescent Study

NCT06631313
completednot_applicable

This Study Will Collect Clinical and Patient Reported Experience Data From Participants Requiring Urine Output Management Overnight in the Home Setting.

NCT06666426
completednot_applicable

PureWick™ France and U.S. At-Home Pilot Study

NCT05710718
View all 6 trials

Clinical Trials (6)

Showing 6 of 6 trials
NCT05090722Not Applicable

A Pilot Study to Evaluate PureWick for Nocturia

Suspended
NCT07282860Not Applicable

An Evaluation of the PureWick™ Male External Catheter Versus an Established Comparator Overnight in the Home Setting for Incontinence in Adult Males

Enrolling By Invitation
NCT06631313Not Applicable

PureWick™ Adolescent Study

Completed
NCT06666426Not Applicable

This Study Will Collect Clinical and Patient Reported Experience Data From Participants Requiring Urine Output Management Overnight in the Home Setting.

Completed
NCT05710718Not Applicable

PureWick™ France and U.S. At-Home Pilot Study

Completed
NCT06850259Not Applicable

This Study Will Collect Clinical and Patient Reported Satisfaction Data From Males Requiring Urine Output Management Overnight in the Home Setting.

Completed

All 6 trials loaded

Drug Details

Intervention Type
DEVICE
Total Trials
6