Key Insights

Highlights

Success Rate

78% trial completion

Published Results

34 trials with published results (14%)

Research Maturity

109 completed trials (43% of total)

Clinical Risk Assessment

Based on trial outcomes

High Risk

Score: 72/100

Termination Rate

12.0%

30 terminated out of 251 trials

Success Rate

78.4%

-8.1% vs benchmark

Late-Stage Pipeline

9%

22 trials in Phase 3/4

Results Transparency

31%

34 of 109 completed with results

Key Signals

34 with results78% success30 terminated

Data Visualizations

Phase Distribution

151Total
Not Applicable (96)
P 1 (22)
P 2 (11)
P 3 (14)
P 4 (8)

Trial Status

Completed109
Unknown34
Recruiting30
Terminated30
Withdrawn19
Enrolling By Invitation11

Trial Success Rate

78.4%

Benchmark: 86.5%

Based on 109 completed trials

Clinical Trials (251)

Showing 20 of 20 trials
NCT05329129RecruitingPrimary

OssDsign® Spine Registry Study ("Propel")

NCT06778447Not ApplicableRecruitingPrimary

Clinical Trial Evaluating the Safety and Efficacy of Nucleus Pulposus Allograft in Participants With Degenerative Disc Disease

NCT07254806Phase 3RecruitingPrimary

A Study to Evaluate the Effectiveness of IDCT (Intradiscal Cell Therapy) in Subjects With One Level, Symptomatic Mild to Moderate Lumbar Degenerative Disc Disease

NCT07386548Not ApplicableNot Yet RecruitingPrimary

Biologic Injection For Adults With Lumbar Disc Herniation

NCT03398915Active Not RecruitingPrimary

The European Robotic Spinal Instrumentation (EUROSPIN) Study

NCT05296889Recruiting

Post-Market Clinical Follow-Up Study on the Safety and Performance of Ennovate® Cervical

NCT04214535Not ApplicableActive Not Recruiting

Anterior Cervical Disectomy And Fusion Using The Tritanium® C Anterior Cervical Cage For One Or Two-Levels

NCT04679844Not ApplicableRecruitingPrimary

Post Marketing Study of MagnetOs Easypack Putty Standalone Compared to Demineralized Bone Matrix or Fibers Mixed With Autograft in Patients Undergoing Posterolateral Lumbar Fusion

NCT05508360Not ApplicableRecruitingPrimary

"Lumbar Operatively Inserted PerQdisc Artificial Implant Following Nulcectomy" (LOPAIN2)

NCT05182489Not ApplicableActive Not Recruiting

Adaptix RCT Evaluating Adaptix™ Versus PEEK Cages

NCT05037968Not ApplicableRecruitingPrimary

MagnetOs Flex Matrix Compared to Trinity Elite Mixed With Local Autograft in Patients Undergoing up to Four-level Instrumented Posterolateral Fusion

NCT07017634Phase 3Not Yet RecruitingPrimary

Efficacy and Safety of Novosis Putty in Transforaminal Lumbar Interbody Fusion for Patients With Lumbar Degenerative Disc Disease

NCT05029726Phase 4Recruiting

Regional Anesthesia in Minimally Invasive Lumbar Spine Surgery

NCT06438471Phase 1Recruiting

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

NCT06053242Phase 1Recruiting

Safety, Tolerability, and Effectiveness of Intramuscular Injection of CELZ-201-DDT for the Treatment of Chronic Lower Back Pain

NCT05701059Recruiting

Comparison of Artificial Disc Implants in Cervical Disc Arthroplasty

NCT06199999Phase 2Completed

Erector Spinae Plane Block vs Local Infiltration Following Fusion Surgery

NCT04984629Not ApplicableCompletedPrimary

Study of the ReGelTec HYDRAFIL System

NCT04416321Not ApplicableCompletedPrimary

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

NCT06115512Phase 3Active Not RecruitingPrimary

A Phase 3 Study of AGA111 in Patients With Degenerative Disc Disease Undergoing Lumbar Interbody Fusion

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