Success Metrics

Clinical Success Rate
50.0%

Based on 3 completed trials

Completion Rate
50%(3/6)
Active Trials
0(0%)
Results Posted
0%(0 trials)
Terminated
3(50%)

Phase Distribution

Ph not_applicable
3
50%

Phase Distribution

0

Early Stage

0

Mid Stage

0

Late Stage

Phase Distribution3 total trials
N/ANon-phased studies
3(100.0%)

Highest Phase Reached

Unknown

Trial Status & Enrollment

Completion Rate

50.0%

3 of 6 finished

Non-Completion Rate

50.0%

3 ended early

Currently Active

0

trials recruiting

Total Trials

6

all time

Status Distribution
Completed(3)
Terminated(3)

Detailed Status

Completed3
Terminated3

Development Timeline

Analytics

Development Status

Total Trials
6
Active
0
Success Rate
50.0%
Most Advanced
N/A

Trials by Phase

N/A3 (100.0%)

Trials by Status

completed350%
terminated350%

Recent Activity

0 active trials
Showing 5 of 6
completednot_applicable

Impact of NOL Intraoperative Guided Fentanyl Analgesia vs SCC for Elective Major Abdominal Surgery

NCT03970291
completed

Nociception-Level (NOL) for the Assessment of Pain in Patient Unable to Self-Report

NCT04581642
terminatednot_applicable

Performance Assessment Of The PMD-200 In Subjects With Degenerative Lumbar Spine Disease Who Requires Surgical Procedure

NCT03389048
terminatednot_applicable

Performance Assessment of the PMD-200 in Subjects at Neurointensive Care Unit

NCT03452163
completed

Performance Assessment of the PMD-200 in Subjects Requiring Surgery Under General Anesthesia

NCT03466138
View all 6 trials

Clinical Trials (6)

Showing 6 of 6 trials
NCT03970291Not Applicable

Impact of NOL Intraoperative Guided Fentanyl Analgesia vs SCC for Elective Major Abdominal Surgery

Completed
NCT04581642

Nociception-Level (NOL) for the Assessment of Pain in Patient Unable to Self-Report

Completed
NCT03389048Not Applicable

Performance Assessment Of The PMD-200 In Subjects With Degenerative Lumbar Spine Disease Who Requires Surgical Procedure

Terminated
NCT03452163Not Applicable

Performance Assessment of the PMD-200 in Subjects at Neurointensive Care Unit

Terminated
NCT03466138

Performance Assessment of the PMD-200 in Subjects Requiring Surgery Under General Anesthesia

Completed
NCT03276260

Evaluation of Medasense's PMD-200 During Surgery and Post Anesthesia Care

Terminated

All 6 trials loaded

Drug Details

Intervention Type
DEVICE
Total Trials
6