Key Insights

Highlights

Success Rate

82% trial completion

Clinical Risk Assessment

Based on trial outcomes

High Risk

Score: 59/100

Termination Rate

10.8%

4 terminated out of 37 trials

Success Rate

81.8%

-4.7% vs benchmark

Late-Stage Pipeline

3%

1 trials in Phase 3/4

Results Transparency

44%

8 of 18 completed with results

Key Signals

8 with results82% success

Data Visualizations

Phase Distribution

26Total
Not Applicable (24)
P 1 (1)
P 3 (1)

Trial Status

Completed18
Unknown5
Recruiting5
Withdrawn4
Terminated4
Enrolling By Invitation1

Trial Success Rate

81.8%

Benchmark: 86.5%

Based on 18 completed trials

Clinical Trials (37)

Showing 20 of 20 trials
NCT06750874Not ApplicableCompleted

Perioperative ACT for Preventing CPSP

NCT07023393Not ApplicableWithdrawn

Proprio Spine Measurement Tool

NCT06438471Phase 1Recruiting

Novel Soluble Epoxide Hydrolase Inhibitor for Neuropathic Pain in Patients With Spinal Cord Injury

NCT05110833Enrolling By Invitation

Dose Responsiveness as a Measure of Clinical Effectiveness During Neuromonitored Spine Surgery

NCT05238740Not ApplicableRecruitingPrimary

Comparison of Radiographic Fusion Rate and Clinical Outcome of ALIF and XLIF Performed With Either Recombinant Human Bone Morphogenetic Protein-2 or ViviGen®

NCT04883411Not ApplicableRecruiting

CEM-Plate and CEM-Cage First-In-Human Use Efficacy Study

NCT05356286Not ApplicableRecruiting

Recording of Intraoperative Spinal Cord Stimulation and Monitoring

NCT03425682CompletedPrimary

ViBone in Cervical and Lumbar Spine Fusion

NCT05306665Not ApplicableRecruiting

PREventing Pain After Surgery

NCT05098431Not ApplicableWithdrawn

Comparison of Three Approaches of Electrode Placement to Detect Changes in Motor Evoked Potentials During Spine Surgery

NCT03945461Not ApplicableCompletedPrimary

Return of Bowel Function After One or Two Level Anterior Lumbar Interbody Fusion With Chewing Gum

NCT04007094Not ApplicableTerminated

Single-Armed Use of ViviGen Cellular Bone Matrix in Patients Undergoing Posterolateral Lumbar Surgery

NCT02403453Terminated

RHINE™ Cervical Disc Clinical Study: A Prospective Observational Study for Patients Requiring 1-2 Level C-spine Surgery

NCT02700451Not ApplicableCompleted

Post-op Acetaminophen vs NSAID Use on Lumbar Spinal Fusion Outcomes

NCT02926391Completed

UNiD 3D VBR Register

NCT05768438Not ApplicableUnknownPrimary

Mulligan Mobilizations and McKenzie Exercises Along With Neural Mobilizations in Cervical Spondylosis

NCT04591249Not ApplicableCompleted

Physical Activity Intervention for Patients Following Lumbar Spine Surgery

NCT03826056Not ApplicableCompleted

Neurology Inpatient Clinical Education Trial

NCT02808234Not ApplicableUnknown

Study of Nucel for One and Two Level Lumbar Interbody Fusion

NCT02628210Not ApplicableCompletedPrimary

Interbody Spacers With map3® Cellular Allogeneic Bone Graft in Anterior or Lateral Lumbar Interbody Fusion

Scroll to load more

Research Network

Activity Timeline