Key Insights

Highlights

Success Rate

75% trial completion

Clinical Risk Assessment

Based on trial outcomes

High Risk

Score: 72/100

Termination Rate

10.3%

3 terminated out of 29 trials

Success Rate

75.0%

-11.5% vs benchmark

Late-Stage Pipeline

0%

0 trials in Phase 3/4

Results Transparency

33%

3 of 9 completed with results

Key Signals

3 with results75% success

Data Visualizations

Phase Distribution

17Total
Not Applicable (17)

Trial Status

Completed9
Enrolling By Invitation4
Active Not Recruiting4
Unknown3
Terminated3
Withdrawn2

Trial Success Rate

75.0%

Benchmark: 86.5%

Based on 9 completed trials

Clinical Trials (29)

Showing 20 of 20 trials
NCT01433367TerminatedPrimary

A Clinical Trial Evaluating a Total Disc Replacement in Patients With Cervical Disc Disease

NCT04770571Enrolling By Invitation

Posterior Cervical Fixation Study

NCT05258435Active Not RecruitingPrimary

Long-term Assessment of the Safety and Performance of the NuVasive Simplify Disc

NCT05066711Enrolling By Invitation

NuVasive® ACP System Study

NCT05691231Enrolling By InvitationPrimary

Long-Term Assessment of the Safety and Performance of the NuVasive Simplify Disc at Two Levels

NCT07287449Not ApplicableNot Yet RecruitingPrimary

A Multi-Center, Prospective Historically Controlled Clinical Trial Comparing the Safety and Effectiveness of Triadyme-C to a Total Disc Replacement Control Cohort in the Treatment of Symptomatic Cervical Disc Disease (SCDD) at a Single Level

NCT06240221Enrolling By InvitationPrimary

A Clinical Registry to Track the Real World Use of the Saber-C® Cervical Fusion Device

NCT03541681Not ApplicableWithdrawn

Repeated Transforaminal Anesthetic Injections With or Without Glucocorticoid in Patients With Cervical Radiculopathy

NCT06601634Recruiting

Predictors of Axial Pain Improvement After Anterior Cervical Discectomy and Fusion

NCT04547959Not ApplicableCompleted

Prospective Clinical Study to Evaluate the Efficacy of the Stand-alone Cervical Interbody Cage C-CURVE ( Titanium) Manufactured by MEDICREA®

NCT04597112Not ApplicableCompleted

Effect of Myofascial Release Technique in Patients with Unilateral Cervical Radiculopathy

NCT06102681Not ApplicableSuspended

Examination of the Effect of Early Mobilization on Postoperative Recovery, Pain, Quality of Life and Complication Development in Elective Minimally Invasive Spine Surgery

NCT04520776Not ApplicableActive Not RecruitingPrimary

A Clinical Trial Comparing the BAGUERA C to the Marketed Mobi-C® for the Treatment of Single Level Cervical Disc Disease

NCT03036007Not ApplicableActive Not RecruitingPrimary

Physiotherapy After Anterior Cervical Spine Surgery

NCT04564885Not ApplicableActive Not RecruitingPrimary

A Clinical Trial Comparing the BAGUERA C to the Marketed Mobi-C® for the Treatment of Cervical Disc Disease at 2 Contiguous Levels

NCT04623593Not ApplicableRecruiting

Cervical Arthroplasty Cost Effectiveness Study (CACES)

NCT05581186Not ApplicableCompleted

Efficacy of Pulse Electromagnetic Field Therapy (PEMF) in Patients With Nonspecific Chronic Neck Pain

NCT03786432Not ApplicableTerminated

Prospective Study of Fusion Rates Using Spira-C Device for Anterior Cervical Discectomy and Fusion Surgery

NCT05717010CompletedPrimary

Is There a Risk of Perioperative Stroke Due to the Retraction Used During Anterior Cervical Discectomy?

NCT04734977Not ApplicableCompleted

Clinical Effectiveness of High-Intensity Laser Therapy in Patients With Cervical Radiculopathy:

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