Key Insights

Highlights

Success Rate

94% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 40/100

Termination Rate

2.4%

1 terminated out of 42 trials

Success Rate

94.1%

+7.6% vs benchmark

Late-Stage Pipeline

19%

8 trials in Phase 3/4

Results Transparency

19%

3 of 16 completed with results

Key Signals

3 with results94% success

Data Visualizations

Phase Distribution

28Total
Not Applicable (16)
P 1 (1)
P 2 (3)
P 3 (3)
P 4 (5)

Trial Status

Completed16
Unknown9
Recruiting6
Withdrawn3
Enrolling By Invitation3
Not Yet Recruiting2

Trial Success Rate

94.1%

Benchmark: 86.5%

Based on 16 completed trials

Clinical Trials (42)

Showing 20 of 20 trials
NCT05444751Phase 3Enrolling By Invitation

GA + ESP vs. SA + ESP in Lumbar Decompression Surgeries

NCT04641039Not ApplicableRecruitingPrimary

Postoperative Scar in the Control Excess of Mobility Induced by Annulus Removal on Inserting a Lumbar Disc Prosthesis

NCT07516613Not Yet RecruitingPrimary

Clinical and MRI Findings in Lumbar Disc Disease

NCT07495501Not Yet RecruitingPrimary

Patient Satisfaction During Lomber Transforaminal Epidural Steroid Injection: The Role of Sedation, Anxiety, and Pain

NCT07454304Not ApplicableCompleted

Ultrasound-Guided vs. Surgeon-Performed (Free-hand) Erector Spinae Plane Block

NCT06825390Not ApplicableRecruiting

AuriculoTherapy NeuroImaging

NCT06462729Phase 1Recruiting

LDGraft in Single Level Anterior Lumbar Interbody Fusion (ALIF)

NCT07338877Enrolling By Invitation

RenewDisc Trial: Endoscopic Discectomy and Autologous Stem Cell Therapy for Discogenic Low Back Pain

NCT07268885Phase 2Completed

PRP Spinoplasty for Chronic Low Back Pain With Multiple Pathologies: A Quasi-Experimental Study

NCT07060235Not ApplicableEnrolling By InvitationPrimary

Development of a Fascial Training Based Mobile Application and Investigation of Its Effectiveness in Patients With Disc Herniation

NCT04042844Phase 2RecruitingPrimary

A Single Dose of BRTX 100 for Patients With Chronic Lumbar Disc Disease (cLDD)

NCT04984213CompletedPrimary

Study of the Long-Term Outcomes of Posterior Spinal Fixation With the Karma Device

NCT03733626Not ApplicableCompleted

Clinical Outcomes Associated With the Use of ViviGen® for the Treatment of Lumbar Degenerative Disc Disease

NCT06989632Recruiting

Total Lumbar Disc Prosthesis and Subsequent Work Activity at at Least Five Years After Total Lumbar Disc Replacement

NCT03060434Phase 4Active Not Recruiting

Pentoxifylline and Lumbar Radiculopathy

NCT05299762Recruiting

A Post Market Surveillance on INFUSE Bone Graft

NCT06777095Not ApplicableCompleted

Effects of Kinesio Taping on Pain, Endurance, Proprioception, Mobility and Disability in Lumbar Disc Herniation

NCT03745040Phase 4Suspended

Liposomal Bupivacaine in One-level Instrumented Posterior Spinal Fusion

NCT05345249Phase 4Completed

Erector Spinae Plane Block as Pain Management After Lumbar Fusion Surgery

NCT04587401Not ApplicableCompletedPrimary

The Effects of Anesthesia on Cerebral Perfusion in Patients With High Blood Pressure

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