Key Insights

Highlights

Success Rate

88% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 50/100

Termination Rate

7.0%

3 terminated out of 43 trials

Success Rate

87.5%

+1.0% vs benchmark

Late-Stage Pipeline

9%

4 trials in Phase 3/4

Results Transparency

10%

2 of 21 completed with results

Key Signals

2 with results88% success

Data Visualizations

Phase Distribution

28Total
Not Applicable (17)
P 1 (5)
P 2 (2)
P 4 (4)

Trial Status

Completed21
Withdrawn5
Recruiting5
Active Not Recruiting3
Unknown3
Terminated3

Trial Success Rate

87.5%

Benchmark: 86.5%

Based on 21 completed trials

Clinical Trials (43)

Showing 20 of 20 trials
NCT05029726Phase 4Recruiting

Regional Anesthesia in Minimally Invasive Lumbar Spine Surgery

NCT07410871CompletedPrimary

Degenerative Spondylolisthesis Accompanying LSS: Do We Need Fusion?

NCT04689880Completed

XLIF Decade Plate System Study

NCT04418830Enrolling By Invitation

Lumbar Interbody Implant Study

NCT04418817Completed

Modulus in XLIF Study

NCT07245940Not Yet Recruiting

Assessing Safety of Cervical Spine Fusion With NMP®

NCT06000319Enrolling By Invitation

Natural Matrix Protein™ (NMP™) Fibers in Cervical and Lumbar Interbody Fusion

NCT03570801Not ApplicableActive Not Recruiting

SLIP II Registry: Spinal Laminectomy Versus Instrumented Pedicle Screw Fusion

NCT03115983Not ApplicableActive Not RecruitingPrimary

LimiFlex Clinical Trial for the Treatment of Degenerative Spondylolisthesis With Spinal Stenosis

NCT06447194Phase 1Withdrawn

Effect of RECK in Posterior Spinal Fusion

NCT07050290Not ApplicableRecruiting

Restoring Segmental Lumbar Lordosis After Failed Previous Fusion at the Same Level

NCT03733626Not ApplicableCompleted

Clinical Outcomes Associated With the Use of ViviGen® for the Treatment of Lumbar Degenerative Disc Disease

NCT05375201Not ApplicableCompleted

Clinical Decision-Making and Virtual Reality Exercise

NCT06394089RecruitingPrimary

Effect of Degenerative Spondylolisthesis on the Clinical Outcome of Unilateral Biportal Endoscopy for Lumbar Spinal Stenosis: Study Protocol

NCT05538416RecruitingPrimary

Short-term Clinical Outcome of Cortical Bone Trajectory Compared With the Traditional "Open" and Minimal Invasive Posterior Lumbar Interbody Fusion

NCT04764825Phase 4Terminated

Methadone for Spinal Fusion Surgery.

NCT06532968Not ApplicableCompleted

Clinical Evaluation of Orion Lamina Cover in Patients Undergoing Lumbar Laminectomy With Instrumented Fusion

NCT05114135Not ApplicableCompleted

TLIF Osteo3 ZP Putty Study (Also Known as the TOP Fusion Study)

NCT05993195CompletedPrimary

Re-operation Rates of Concorde Bullet Device Versus Conduit Titanium Interbody Graft for Lumbar Fusion

NCT06320899Not ApplicableRecruiting

Mid- or High-flex Rods Versus Low-flex Rods of SpineShape System IV for Treatment of Degenerative Lumbar Spine Diseases

Scroll to load more

Research Network

Activity Timeline