Procedure
Posterolateral Fusion
Posterolateral Fusion is a medical procedure with 5 clinical trials. Historical success rate of 100.0%.
Total Trials
5
Max Phase
—
Type
PROCEDURE
Molecule
—
Success Metrics
Clinical Success Rate
100.0%
Based on 4 completed trials
Completion Rate
100%(4/4)
Active Trials
0(0%)
Results Posted
50%(2 trials)
Phase Distribution
Ph phase_4
1
20%
Ph not_applicable
4
80%
Phase Distribution
0
Early Stage
0
Mid Stage
1
Late Stage
Phase Distribution5 total trials
Phase 4Post-market surveillance
1(20.0%)
N/ANon-phased studies
4(80.0%)
Highest Phase Reached
Phase 4Trial Status & Enrollment
Completion Rate
100.0%
4 of 4 finished
Non-Completion Rate
0.0%
0 ended early
Currently Active
0
trials recruiting
Total Trials
5
all time
Status Distribution
Completed(4)
Other(1)
Detailed Status
Completed4
unknown1
Development Timeline
Analytics
Development Status
Total Trials
5
Active
0
Success Rate
100.0%
Most Advanced
Phase 4
Trials by Phase
Phase 41 (20.0%)
N/A4 (80.0%)
Trials by Status
unknown120%
completed480%
Recent Activity
0 active trials
Showing 5 of 5
completednot_applicable
A Pre-market Study to Evaluate b.Bone for Posterolateral Fusion (b.Spine Clinical Trial).
NCT05906394
completednot_applicable
Sagittal Parameters After Mono Segmental Lumber Fusion: Interbody Versus Postrolateral Fusion
NCT03877341
completednot_applicable
Accell Evo3™ Demineralized Bone Matrix in Instrumented Lumbar Spine Fusion
NCT02018445
completednot_applicable
OsteoStrux™ Collagen Ceramic Scaffold in Instrumented Lumbar Spine Fusion
NCT01873586
unknownphase_4
Interbody vs Instrumented Posterolateral Fusion Following Decompression for Lumbar Spinal Stenosis With Degenerative Spondylolisthesis
NCT01921530
Clinical Trials (5)
Showing 5 of 5 trials
NCT05906394Not Applicable
A Pre-market Study to Evaluate b.Bone for Posterolateral Fusion (b.Spine Clinical Trial).
NCT03877341Not Applicable
Sagittal Parameters After Mono Segmental Lumber Fusion: Interbody Versus Postrolateral Fusion
NCT02018445Not Applicable
Accell Evo3™ Demineralized Bone Matrix in Instrumented Lumbar Spine Fusion
NCT01873586Not Applicable
OsteoStrux™ Collagen Ceramic Scaffold in Instrumented Lumbar Spine Fusion
NCT01921530Phase 4
Interbody vs Instrumented Posterolateral Fusion Following Decompression for Lumbar Spinal Stenosis With Degenerative Spondylolisthesis
All 5 trials loaded
Drug Details
- Intervention Type
- PROCEDURE
- Total Trials
- 5