Key Insights

Highlights

Success Rate

41% trial completion

Clinical Risk Assessment

Based on trial outcomes

High Risk

Score: 80/100

Termination Rate

39.0%

16 terminated out of 41 trials

Success Rate

40.7%

-45.8% vs benchmark

Late-Stage Pipeline

44%

18 trials in Phase 3/4

Results Transparency

27%

3 of 11 completed with results

Key Signals

3 with results41% success16 terminated

Data Visualizations

Phase Distribution

26Total
Not Applicable (8)
P 3 (2)
P 4 (16)

Trial Status

Terminated16
Completed11
Active Not Recruiting10
Recruiting2
Unknown1
Withdrawn1

Trial Success Rate

40.7%

Benchmark: 86.5%

Based on 11 completed trials

Clinical Trials (41)

Showing 20 of 20 trials
NCT06564636Active Not Recruiting

A Multi-Centre Study in Patients Undergoing Total Hip Arthroplasty With the Smith+Nephew CATALYSTEM™ Primary Hip System

NCT03396224Active Not Recruiting

Avenir® Cemented Hip Stem - PMCF

NCT01285843Not ApplicableCompleted

Periprosthetic Bone Mineral Density After Total Hip Arthroplasty Performed Through a Minimally Invasive Anterior Approach (AMIS) With Either an AMIStem or a Quadra Femoral Component

NCT02748408Recruiting

The Medacta International SMS Post-Marketing Surveillance Study

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

NCT02783274Not ApplicableCompleted

Actis Total Hip System 2 Year Follow-up

NCT04349046Active Not Recruiting

Exception Cementless Hip Stem

NCT03372278Active Not Recruiting

PMCF Study on the Safety and Performance of the Zimmer® Maxera™ Acetabular System in Total Hip Arthroplasty

NCT04997005Active Not Recruiting

The Medacta International AMIStem-P Post-Marketing Surveillance Study

NCT03226808Not ApplicableActive Not Recruiting

Vivacit-E Post-market Follow-up Study

NCT01107340Not ApplicableActive Not Recruiting

AMIStem Primary Hip System Prospective Post-marketing Multi-centre Surveillance Study

NCT04117685Recruiting

Global Hip Dysplasia Registry

NCT03357445Not ApplicableActive Not Recruiting

AVANTAGE® RELOAD Double Mobility Acetabular Cup -Clinical Study

NCT06209255CompletedPrimary

Pelvic Osteotomy Of The Total Hip Replacement

NCT02196818Terminated

A Multi-centre, Prospective Surveillance to Assess Mid-term Performance of the Mpact Cup

NCT04212039Not ApplicableCompletedPrimary

Pericapsular Nerve Group (PENG) Block for Congenital Hip Dislocation Surgery

NCT00546598Phase 4Terminated

Post-approval Study of the DURALOC® Option Ceramic-on-Ceramic Hip Prosthesis System

NCT03949686Not ApplicableCompletedPrimary

Erector Spinae Plane Block for Congenital Hip Dislocation Surgery

NCT02162186Completed

Clinical and Radiographic Outcomes of the Corin Tri-Fit Total Hip Replacement

Scroll to load more

Research Network

Activity Timeline