Registry-listed formulations

This catalogue entry has no confirmed scientific concept.

Each study is counted once in the molecule profile. Registry products remain separate. Naming an ingredient does not establish that products are interchangeable or what participants received.

2 source entries across 2 studies. This list may not include all unresolved or historical entries.

  • Local anesthetic infusionRegistry intervention

    Linked study entry; product equivalence not established

    View study and source
  • Local anesthetic infusionRegistry intervention

    Linked study entry; product equivalence not established

    View study and source

Success Metrics

Clinical Success Rate
100.0%

Based on 1 completed trials

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

Phase Distribution

Phase 4
2
100%

Phase Distribution

0

Early Stage

0

Mid Stage

2

Late Stage

Phase Distribution2 total trials
Phase 4Post-market surveillance
2(100.0%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

50.0%

1 of 2 finished

Non-Completion Rate

50.0%

1 ended early

Currently Active

0

trials recruiting

Total Trials

2

all time

Status Distribution
Completed(1)
Terminated(1)

Detailed Status

Withdrawn1
Completed1

Development Timeline

Analytics

Development Status

Total Trials
2
Active
0
Success Rate
100.0%
Most Advanced
Phase 4

Trials by Phase

Phase 42 (100.0%)

Trials by Status

withdrawn150%
completed150%

Recent Activity

0 active trials
Showing 2 of 2
completedphase_4

Stimulating Catheter for Lumbar Plexus Block: Better Postoperative Analgesia?

NCT02162121
withdrawnphase_4

Total Knee Prosthesis With Continuous Block of Adductor Canal and Outcome

NCT02082067

Clinical Trials (2)

Showing 2 of 2 trials
NCT02162121Phase 4

Stimulating Catheter for Lumbar Plexus Block: Better Postoperative Analgesia?

Completed
NCT02082067Phase 4

Total Knee Prosthesis With Continuous Block of Adductor Canal and Outcome

Withdrawn

All 2 trials loaded

Drug Details

Intervention Type
Procedure
Total Trials
2