Key Insights

Highlights

Success Rate

89% trial completion (above average)

Published Results

25 trials with published results (13%)

Research Maturity

87 completed trials (45% of total)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 50/100

Termination Rate

5.7%

11 terminated out of 193 trials

Success Rate

88.8%

+2.3% vs benchmark

Late-Stage Pipeline

10%

19 trials in Phase 3/4

Results Transparency

29%

25 of 87 completed with results

Key Signals

25 with results89% success11 terminated

Data Visualizations

Phase Distribution

119Total
Not Applicable (92)
Early P 1 (3)
P 1 (1)
P 2 (4)
P 3 (4)
P 4 (15)

Trial Status

Completed87
Unknown33
Recruiting27
Not Yet Recruiting12
Active Not Recruiting11
Terminated11

Trial Success Rate

88.8%

Benchmark: 86.5%

Based on 87 completed trials

Clinical Trials (193)

Showing 20 of 20 trials
NCT03072927RecruitingPrimary

MILD® Percutaneous Image-Guided Lumbar Decompression: A Medicare Claims Study

NCT07562035Not ApplicableCompletedPrimary

Endoscopic Versus Conventional Lumbar Decompression for Lumbar Canal Stenosis

NCT05058287Phase 3Recruiting

Lumbar Steroid Use in Patients Undergoing Posterior Lumbar Decompression

NCT07001982CompletedPrimary

Lumbar Spinal Stenosis and Central Sensitization

NCT06959355CompletedPrimary

Frailty and Associated Factors in Lumbar Spinal Stenosis

NCT07489508CompletedPrimary

Retrospective Comparison of Tubular Decompression ± Rhizotomy Versus TLIF in Lumbar Spinal Stenosis

NCT07489001RecruitingPrimary

Opioid Free and Opioid Based Anesthesia in Elective Lumbar Spine Surgery

NCT04992572Early Phase 1RecruitingPrimary

Study Comparing Local/ MAC Anesthesia in Lumbar Decompression

NCT07469020Not ApplicableNot Yet Recruiting

CLE-PAD : Prevalence of PAD in Patients With Surgically Lumbar Spinal Stenosis

NCT03918512WithdrawnPrimary

Development and Validation of a Questionnaire for Assessing Activity Limitation in Patients With Lumbar Spinal Stenosis : The Cochin L3S Questionnaire

NCT07233798RecruitingPrimary

Presence of Dural Pulsation in Patients Diagnosed With Lumbar Spinal Stenosis

NCT04192591Not ApplicableActive Not RecruitingPrimary

A 5-year Superion™ IDS Clinical Outcomes Post-Approval Evaluation (SCOPE)

NCT04594980Not ApplicableCompletedPrimary

Minimally Invasive Decompression and Fusion Versus Open for Degenerative Lumbar Stenosis

NCT07445477Not ApplicableCompletedPrimary

Erector Spinae Plane vs Caudal Epidural Steroid in Lumbar Spinal Stenosis Resistant to Conservative Therapy

NCT06654856CompletedPrimary

The Effectiveness and Safety of Dong-A Opalmon® Tablet in Patients With Acquired Lumbar Spinal Stenosis

NCT06987409Not ApplicableNot Yet RecruitingPrimary

Continuous Erector Spinae Block for Analgesia Following Lumbar Decompression

NCT05029726Phase 4RecruitingPrimary

Regional Anesthesia in Minimally Invasive Lumbar Spine Surgery

NCT07410871Completed

Degenerative Spondylolisthesis Accompanying LSS: Do We Need Fusion?

NCT06335511CompletedPrimary

Decompression Versus Instrumented Fusion for Lumbar Degenerative Disease. Clinical and Biomechanical Outcome Study

NCT06763224Completed

Prevalence of Neuropathic Pain After Non-instrumented Lumbar Spinal Surgery

Scroll to load more

Research Network

Activity Timeline