Success Metrics

Clinical Success Rate
100.0%

Based on 2 completed trials

Completion Rate
100%(2/2)
Active Trials
0(0%)
Results Posted
0%(0 trials)

Phase Distribution

Ph not_applicable
4
100%

Phase Distribution

0

Early Stage

0

Mid Stage

0

Late Stage

Phase Distribution4 total trials
N/ANon-phased studies
4(100.0%)

Highest Phase Reached

Unknown

Trial Status & Enrollment

Completion Rate

66.7%

2 of 3 finished

Non-Completion Rate

33.3%

1 ended early

Currently Active

0

trials recruiting

Total Trials

4

all time

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

Detailed Status

Completed2
Withdrawn1
unknown1

Development Timeline

Analytics

Development Status

Total Trials
4
Active
0
Success Rate
100.0%
Most Advanced
N/A

Trials by Phase

N/A4 (100.0%)

Trials by Status

completed250%
withdrawn125%
unknown125%

Recent Activity

0 active trials
Showing 4 of 4
unknownnot_applicable

Acute Post-operative Pain in Colon Resections

NCT03403842
completednot_applicable

Femoral Neuropathy After Anterior Cruciate Ligament Reconstruction: Femoral Nerve Block vs Patient-controlled Analgesia (PCA)

NCT01321138
withdrawnnot_applicable

Incidence of Brachial Plexus Injury After Rotator Cuff Repair With Continuous Interscalene Block

NCT01334632
completednot_applicable

Functional Restoration After Abdominal and Pelvic Laparoscopic Surgery: Effect of Perioperative Intravenous Lidocaine

NCT00982618

Clinical Trials (4)

Showing 4 of 4 trials
NCT03403842Not Applicable

Acute Post-operative Pain in Colon Resections

Unknown
NCT01321138Not Applicable

Femoral Neuropathy After Anterior Cruciate Ligament Reconstruction: Femoral Nerve Block vs Patient-controlled Analgesia (PCA)

Completed
NCT01334632Not Applicable

Incidence of Brachial Plexus Injury After Rotator Cuff Repair With Continuous Interscalene Block

Withdrawn
NCT00982618Not Applicable

Functional Restoration After Abdominal and Pelvic Laparoscopic Surgery: Effect of Perioperative Intravenous Lidocaine

Completed

All 4 trials loaded

Drug Details

Intervention Type
PROCEDURE
Total Trials
4