Key Insights

Highlights

Success Rate

71% trial completion

Published Results

14 trials with published results (11%)

Research Maturity

55 completed trials (43% of total)

Clinical Risk Assessment

Based on trial outcomes

High Risk

Score: 72/100

Termination Rate

17.2%

22 terminated out of 128 trials

Success Rate

71.4%

-15.1% vs benchmark

Late-Stage Pipeline

9%

12 trials in Phase 3/4

Results Transparency

25%

14 of 55 completed with results

Key Signals

14 with results71% success22 terminated

Data Visualizations

Phase Distribution

83Total
Not Applicable (64)
P 1 (4)
P 2 (3)
P 3 (4)
P 4 (8)

Trial Status

Completed55
Terminated22
Unknown19
Recruiting12
Active Not Recruiting7
Not Yet Recruiting5

Trial Success Rate

71.4%

Benchmark: 86.5%

Based on 55 completed trials

Clinical Trials (128)

Showing 20 of 20 trials
NCT06750874Not ApplicableCompleted

Perioperative ACT for Preventing CPSP

NCT07547969Not ApplicableNot Yet RecruitingPrimary

Effect of Hip Extension Mobilization on Functional Disability in Patients With Spondylolisthesis

NCT07514806Not ApplicableCompletedPrimary

Ultrasound-Guided Erector Spinae Plane Block for Postoperative Pain Control in Lumbar Spondylolisthesis Surgery

NCT03398915Active Not Recruiting

The European Robotic Spinal Instrumentation (EUROSPIN) Study

NCT06093477Not ApplicableRecruiting

Studying Melatonin and Recovery in Teens

NCT05071144Recruiting

Advanced SPinal Innovations With Robotics and Enabling Technology Registry

NCT05182489Not ApplicableActive Not Recruiting

Adaptix RCT Evaluating Adaptix™ Versus PEEK Cages

NCT07419256Not ApplicableCompleted

Rehabilitation Programs in Grade I-II Spondylolisthesis

NCT05583864Not ApplicableActive Not Recruiting

Lumbar Fusion With Porous Versus Non-Porous Cages

NCT04637802Not ApplicableCompleted

Digital Health Psychosocial Intervention for Adolescent Spine Surgery Preparation and Recovery

NCT04416321Not ApplicableCompleted

A Clinical Study to Evaluate Safety and Performance of PEEK-OPTIMA™ HA Enhanced.

NCT01024699CompletedPrimary

XLIF® vs. MAS®TLIF for the Treatment of Symptomatic Lumbar Degenerative Spondylolisthesis With or Without Central Stenosis.

NCT05566704Completed

Retrospective Modulus ALIF Study

NCT03649490Enrolling By Invitation

Advanced Materials Science in XLIF Study

NCT04420143Completed

MLX/XLX ACR Expandable Lumbar Interbody Implants

NCT07242976Not ApplicableNot Yet Recruiting

Evaluation of Balance Using the Biodex Balance System Among Different Subcategories of Low Back Pain

NCT04684901Not ApplicableEnrolling By Invitation

Effectiveness of AlloWrap® for the Reduction of Inflammation in ACDF Procedures

NCT06398600Not ApplicableCompletedPrimary

Caudal Block Versus Quadratus Lumborum Plane Block in Lumbar Surgery

NCT05366140RecruitingPrimary

Thoracic-Lumbar Arthrodesis- Implanet Jazz

NCT06355791Not ApplicableRecruiting

Post-Market Clinical Study of Functional Motion Outcomes in Subjects Treated With the Minuteman Device

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