Success Metrics

Clinical Success Rate
83.3%

Based on 5 completed trials

Completion Rate
83%(5/6)
Active Trials
0(0%)
Results Posted
20%(1 trials)
Terminated
1(13%)

Phase Distribution

Ph phase_4
1
13%
Ph not_applicable
6
75%

Phase Distribution

0

Early Stage

0

Mid Stage

1

Late Stage

Phase Distribution7 total trials
Phase 4Post-market surveillance
1(14.3%)
N/ANon-phased studies
6(85.7%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

83.3%

5 of 6 finished

Non-Completion Rate

16.7%

1 ended early

Currently Active

0

trials recruiting

Total Trials

8

all time

Status Distribution
Completed(5)
Terminated(1)
Other(2)

Detailed Status

Completed5
unknown2
Terminated1

Development Timeline

Analytics

Development Status

Total Trials
8
Active
0
Success Rate
83.3%
Most Advanced
Phase 4

Trials by Phase

Phase 41 (14.3%)
N/A6 (85.7%)

Trials by Status

unknown225%
completed563%
terminated113%

Recent Activity

0 active trials
Showing 5 of 8
completednot_applicable

Radiological Investigation of Bile Duct Obstruction

NCT02351492
unknownnot_applicable

ACCESS HD: Comparing Catheters to Fistulas in Elderly Patients Starting Hemodialysis

NCT02675569
completednot_applicable

Feasibility Study of Photovaporisation of Prostate With a Limitated Length of Catheterization of 3 Hours

NCT02401581
completednot_applicable

Open Technique Interpectoral Catheter for Postoperative Analgesia in Modified Radical Mastectomy

NCT03204708
terminatedphase_4

Ripening Interventions: Prostaglandins vs EASI Catheter

NCT00383942
View all 8 trials

Clinical Trials (8)

Showing 8 of 8 trials
NCT02351492Not Applicable

Radiological Investigation of Bile Duct Obstruction

Completed
NCT02675569Not Applicable

ACCESS HD: Comparing Catheters to Fistulas in Elderly Patients Starting Hemodialysis

Unknown
NCT02401581Not Applicable

Feasibility Study of Photovaporisation of Prostate With a Limitated Length of Catheterization of 3 Hours

Completed
NCT03204708Not Applicable

Open Technique Interpectoral Catheter for Postoperative Analgesia in Modified Radical Mastectomy

Completed
NCT00383942Phase 4

Ripening Interventions: Prostaglandins vs EASI Catheter

Terminated
NCT01500655Not Applicable

Ultrasound-Guided Block of the Lateral Femoral Cutaneous Nerve in Pediatric Patients

Completed
NCT00396903

Evaluation of a Standard Epidural Catheter During Clinical Practice

Completed
NCT01019005Not Applicable

Pain Relief After Forefoot Surgery

Unknown

All 8 trials loaded

Drug Details

Intervention Type
DEVICE
Total Trials
8