Key Insights

Highlights

Success Rate

62% trial completion

Clinical Risk Assessment

Based on trial outcomes

High Risk

Score: 59/100

Termination Rate

18.5%

10 terminated out of 54 trials

Success Rate

61.5%

-25.0% vs benchmark

Late-Stage Pipeline

6%

3 trials in Phase 3/4

Results Transparency

56%

9 of 16 completed with results

Key Signals

9 with results62% success

Data Visualizations

Phase Distribution

26Total
Not Applicable (23)
P 4 (3)

Trial Status

Completed16
Active Not Recruiting13
Terminated10
Recruiting6
Withdrawn4
Unknown3

Trial Success Rate

61.5%

Benchmark: 86.5%

Based on 16 completed trials

Clinical Trials (54)

Showing 20 of 20 trials
NCT05773352Active Not Recruiting

Perform® Humeral System - Fracture Study (PFX)

NCT06631638Not ApplicableRecruiting

EMPHASYS Cup Positioning in THA With Non-Invasive Navigation (Velys Hip Navigation (VHN))

NCT02539056Not ApplicableCompleted

The Post-marketing Surveillance to Evaluate the Efficacy and Safety of a CHONDRON (Autologous Cultured Chondrocyte)

NCT02539069Not ApplicableCompleted

The Post-marketing Surveillance to Evaluate the Efficacy of CHONDRON (Autologous Cultured Chondrocyte) by Arthroscopy

NCT05500066Enrolling By Invitation

Tornier HRS (Humeral Reconstruction System) Study (REVIVE)

NCT02255383Not ApplicableActive Not Recruiting

Persona Total Knee Arthroplasty Outcomes Study

NCT05049993Active Not Recruiting

Pyrocarbon Clinical Follow-up Study

NCT05787821Recruiting

Persona OsseoTi Keel Compatibility Study (Total Knee Arthroplasty)

NCT05630053Not ApplicableActive Not Recruiting

Cemented vs Cementless Persona Keel RCT

NCT01064063Not ApplicableCompleted

Randomized Controlled Clinical Evaluation to Compare Vanguard Cruciate Retaining and AGC Total Condylar Knee Implants

NCT02337244Active Not Recruiting

Zimmer POLAR Persona - TKA (EMEA Study)

NCT01542580Active Not Recruiting

A Prospective, Clinical Investigation of the Vanguard 360 Revision Knee

NCT04817969Not ApplicableActive Not Recruiting

Persona Ti-Nidium Post-Market Clinical Follow-up

NCT06012656Active Not Recruiting

Prospective Study for the Evaluation of the Cementless Anatomic Femoral Stem Minimax -Launay

NCT05460715Active Not Recruiting

The Medacta Quadra-P Anteverted Study

NCT02748408Recruiting

The Medacta International SMS Post-Marketing Surveillance Study

NCT05003414Active Not Recruiting

The Medacta International GMK Sphere Cementless Post-Marketing Surveillance Study

NCT06546345Recruiting

Post Market Clinical Follow-Up KeriFlex®

NCT03247023Terminated

Long Term Follow-up of Integra® Cadence™ Total Ankle System in Primary Ankle Joint Replacement

NCT02783274Not ApplicableCompleted

Actis Total Hip System 2 Year Follow-up

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