Key Insights

Highlights

Success Rate

83% trial completion

Clinical Risk Assessment

Based on trial outcomes

High Risk

Score: 62/100

Termination Rate

7.9%

3 terminated out of 38 trials

Success Rate

83.3%

-3.2% vs benchmark

Late-Stage Pipeline

3%

1 trials in Phase 3/4

Results Transparency

13%

2 of 15 completed with results

Key Signals

2 with results83% success

Data Visualizations

Phase Distribution

17Total
Not Applicable (15)
Early P 1 (1)
P 3 (1)

Trial Status

Completed15
Recruiting7
Enrolling By Invitation6
Unknown4
Terminated3
Active Not Recruiting1

Trial Success Rate

83.3%

Benchmark: 86.5%

Based on 15 completed trials

Clinical Trials (38)

Showing 20 of 20 trials
NCT04498806Not ApplicableEnrolling By InvitationPrimary

Activity Monitors as a Measure of Physical Function in Degenerative Cervical Myelopathy

NCT06876012Not ApplicableNot Yet RecruitingPrimary

Impact of Tai Chi in Cervical Myelopathy

NCT05446259RecruitingPrimary

Degenerative Cervical Myelopathy Repository

NCT05066711Enrolling By Invitation

NuVasive® ACP System Study

NCT04770571Enrolling By Invitation

Posterior Cervical Fixation Study

NCT06701422Not ApplicableRecruiting

Targeting Cervical Epidural Spinal Cord Stimulation for Functional Recovery

NCT06893406Not ApplicableRecruitingPrimary

Cervical Myelopathy in Hip Fracture Patients

NCT06475365Not ApplicableEnrolling By Invitation

Salt Water Gargling on Swallowing Following ACDF

NCT06520020Not ApplicableRecruiting

Evaluating Safety and Feasibility of Transcutaneous Spinal Cord Stimulation Following Traumatic and Non-Traumatic Spinal Cord Injury: A Pilot Study

NCT06610175Active Not Recruiting

Quantitative Imaging of Cervical Spinal Structures - the DISC Pilot Study -

NCT05163639Early Phase 1Recruiting

Spinal Cord Associative Plasticity Study

NCT05762055Not ApplicableEnrolling By Invitation

Prospective Comparative Analysis of ACDF vs Fusion Interbody Cages With nanoLOCK Osseointegrative Technology

NCT04381663Enrolling By Invitation

CSS-Assessing the Course of Degenerative Cervical Spinal Stenosis Using Functional Outcomes

NCT05183971RecruitingPrimary

Proprioceptive Deficits in Degenerative Cervical Myelopathy

NCT06486038Not ApplicableRecruitingPrimary

Quatitative MRI of the Spinal Cord in Cervical Myelopathy: Assessment of Microstuctural Damage for Outcome Improvement

NCT03695848CompletedPrimary

Prognostic Value of DTI and fMRI of Cervical Myelopathy

NCT02125981Phase 3CompletedPrimary

The Study About the Efficacy of Oral Limaprost After Surgery for Cervical Myelopathy

NCT04545983Not ApplicableCompletedPrimary

Long-term Follow-up Motion Analysis of ACD Versus ACDA

NCT04968639UnknownPrimary

The Characteristic of Axial Pain and EEG Analysis of Patients After Laminoplasty

NCT04962256CompletedPrimary

ERAS in Posterior Approach of Cervical Spine Operation

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