Key Insights

Highlights

Success Rate

100% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 50/100

Termination Rate

0.0%

0 terminated out of 11 trials

Success Rate

100.0%

+13.5% vs benchmark

Late-Stage Pipeline

9%

1 trials in Phase 3/4

Results Transparency

0%

0 of 1 completed with results

Key Signals

100% success

Data Visualizations

Phase Distribution

8Total
Not Applicable (6)
P 1 (1)
P 4 (1)

Trial Status

Not Yet Recruiting5
Recruiting3
Completed1
Active Not Recruiting1
Withdrawn1

Trial Success Rate

100.0%

Benchmark: 86.5%

Based on 1 completed trials

Clinical Trials (11)

Showing 11 of 11 trials
NCT07705451Not ApplicableNot Yet Recruiting

Virtual Reality for Intraoperative Anxiolysis and Postoperative Agitation in Elderely Hip Arthroplasty Patients

NCT07631091Phase 4Not Yet Recruiting

Post-Operative Spinal Block Duration and Pain Relief After Hip Replacement Surgery: Comparing Single-Shot Spinal Ropivacaine and Bupivacaine

NCT07110324Recruiting

Characteristics of Persistent Pain Composition Following Total Hip or Knee Arthroplasty: a Descriptive Study

NCT07392515Not ApplicableRecruiting

Cognitive and Physical Recovery After Hip Fracture in Frail Patients Using Digital Rehabilitation Technology

NCT07201116Not ApplicableCompletedPrimary

Health-GIS Platform for Hip Replacement Rehabilitation Coordination

NCT03113981Not ApplicableActive Not Recruiting

Osseointegration of THA Grafted by PolyNASS (ACTISURF-CERAFIT® ) Versus Non-grafted THA (CERAFIT®)

NCT07207005Not ApplicableNot Yet RecruitingPrimary

Comparison of Wear Between Two Dual-mobility Acetabular Cups in Patients Undergoing Total Hip Arthroplasty

NCT07109388Not ApplicableNot Yet RecruitingPrimary

Comparison of Pericapsular Nerve Group (PENG) Block With a Combined Femoral, Sciatic, Lateral Femoral Cutaneous Nerve Block for Postoperative Analgesia in Secondary Total Hip Arthroplasty; (REVPET)

NCT06888908RecruitingPrimary

Changes in Perioperative Blood Volume and Fluid Distribution in Patients Undergoing Primary Total Hip Replacement.

NCT06873568Not Yet RecruitingPrimary

Cephalic Femoral Heads Follow Up

NCT01454271Phase 1WithdrawnPrimary

Follow up Study of Patients Undergoing Total Hip Arthroplasty CERAFIT® Grafted With Poly Sodium Styrene Sulfonate

Showing all 11 trials

Research Network

Activity Timeline