Key Insights

Highlights

Success Rate

92% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 40/100

Termination Rate

4.8%

2 terminated out of 42 trials

Success Rate

91.7%

+5.1% vs benchmark

Late-Stage Pipeline

12%

5 trials in Phase 3/4

Results Transparency

14%

3 of 22 completed with results

Key Signals

3 with results92% success

Data Visualizations

Phase Distribution

27Total
Not Applicable (17)
P 2 (5)
P 3 (1)
P 4 (4)

Trial Status

Completed22
Recruiting5
Not Yet Recruiting4
Unknown4
Active Not Recruiting2
Enrolling By Invitation2

Trial Success Rate

91.7%

Benchmark: 86.5%

Based on 22 completed trials

Clinical Trials (42)

Showing 20 of 20 trials
NCT06510205Recruiting

The Study is an Observational Post-market Follow-up Program to Evaluate Long Term (5 Years) Safety of Mentor Breast Implants in Chinese Population

NCT07729735Not ApplicableEnrolling By Invitation

Physiotherapy After Breast Reduction Surgery

NCT04891510Not ApplicableRecruiting

A Comparative Analysis of REVOLVE, LipoGrafter, and Viality in Autologous Fat Grafting During Breast Surgery

NCT07657949Not ApplicableNot Yet Recruiting

SPSIP Block for Pain Control After Breast Reduction Surgery

NCT07657962Not Yet Recruiting

Autologous Free Dermal Graft Support in Superior Pedicle Vertical Scar Reduction Mammaplasty

NCT07628517Not Yet RecruitingPrimary

Custom Breast Implants With 3D Imaging

NCT07623564Enrolling By Invitation

Clinical Study on Tissue Preservation in Breast Augmentation and Reconstruction

NCT06274736Completed

Safety and Performance of Motiva® Sizers

NCT06420323Active Not Recruiting

NovoX®Cup as Primary Dressing After Breast Reduction

NCT03240900Not ApplicableNot Yet RecruitingPrimary

Electrical Stimulation for Improving Postoperative Breast Sensation

NCT06146231Not ApplicableRecruitingPrimary

Motiva Flora® Aesthetic Breast Recon® Clinical Study

NCT06725459Not ApplicableRecruiting

NPWT Reduction Mammaplasty

NCT05171179Phase 3CompletedPrimary

The Use of Pecs Blocks in Combination With Exparel in Breast Reconstruction Surgery

NCT07008339Not ApplicableRecruiting

Impact of Nipple Reconstruction in Mastectomized Patients Using Cross-Linked Hyaluronic Acid Injection.

NCT04715802Active Not Recruiting

Options on the Breast Reconstruction Timing and Method After Removal of Polyacrylamide Hydrogel

NCT04079686Not ApplicableCompleted

Single Dose Versus 24 Hours Antibiotic Prophylaxis in Reduction Mammaplasty

NCT06611644Not ApplicableCompleted

Comparison of ESP and SPSIP Blocks in Breast Surgery

NCT06504173CompletedPrimary

Diced Cartilage in Breast Reconstruction

NCT04931615Phase 4Completed

ARTISS a Single-centre Randomised Control Study

NCT04919317Phase 2Completed

Combination Dexamethasone and Bupivacaine Pain Control in Reduction Mammaplasty

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Research Network

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