Success Metrics

Clinical Success Rate
100.0%

Based on 3 completed trials

Completion Rate
100%(3/3)
Active Trials
1(20%)
Results Posted
0%(0 trials)

Phase Distribution

Ph not_applicable
2
40%

Phase Distribution

0

Early Stage

0

Mid Stage

0

Late Stage

Phase Distribution2 total trials
N/ANon-phased studies
2(100.0%)

Highest Phase Reached

Unknown

Trial Status & Enrollment

Completion Rate

100.0%

3 of 3 finished

Non-Completion Rate

0.0%

0 ended early

Currently Active

1

trials recruiting

Total Trials

5

all time

Status Distribution
Active(1)
Completed(3)
Other(1)

Detailed Status

Completed3
unknown1
Active, not recruiting1

Development Timeline

Analytics

Development Status

Total Trials
5
Active
1
Success Rate
100.0%
Most Advanced
N/A

Trials by Phase

N/A2 (100.0%)

Trials by Status

completed360%
unknown120%
active_not_recruiting120%

Recent Activity

1 active trials
Showing 5 of 5
completednot_applicable

Establishing Baseline Sysmex UF-5000 Flow Cytometer Results in Healthy Men

NCT06951009
completed

First-void Urine Samples for the Follow-up of Women Treated for High-grade Cervical Intraepithelial Neoplasia (CIN)

NCT03542513
unknownnot_applicable

Increase in Response by Offering Self-sampling Devices in Belgian GP Practices to Non-screened Women

NCT04903561
active_not_recruiting

Validation of Human Papillomavirus Assays and Collection Devices for Self-samples and Urine Samples

NCT03064087
completed

Evaluation of the Use of the Colli-Pee Device to Collect First-void Urine for Molecular Detection of STIs

NCT02552914

Clinical Trials (5)

Showing 5 of 5 trials
NCT06951009Not Applicable

Establishing Baseline Sysmex UF-5000 Flow Cytometer Results in Healthy Men

Completed
NCT03542513

First-void Urine Samples for the Follow-up of Women Treated for High-grade Cervical Intraepithelial Neoplasia (CIN)

Completed
NCT04903561Not Applicable

Increase in Response by Offering Self-sampling Devices in Belgian GP Practices to Non-screened Women

Unknown
NCT03064087

Validation of Human Papillomavirus Assays and Collection Devices for Self-samples and Urine Samples

Active Not Recruiting
NCT02552914

Evaluation of the Use of the Colli-Pee Device to Collect First-void Urine for Molecular Detection of STIs

Completed

All 5 trials loaded

Drug Details

Intervention Type
DEVICE
Total Trials
5