C. R. Bard
Trial Pipeline
Real-World Registry of the Rotarex(TM) Rotational Excisional Atherectomy System (XTRACT Registry)
NCT07016698
Study of GalaFLEX LITE™ Scaffold in Treatment of Capsular Contracture After Breast Implant Augmentation
NCT05945329
Post-market Surveillance Study of the BD® WavelinQ™ EndoAVF System
NCT04634916
Prophylactic Reinforcement of Ventral Abdominal Incisions Trial
NCT03911700
Venclose digiRF System Post Market Study
NCT05504070
Post Approval Study Investigating Lutonix Drug Coated Balloon for Treatment of Dysfunctional Arteriovenous Fistulae
NCT03506308
Post Approval Study of the BARD® COVERA™ Arteriovenous (AV) Stent Graft
NCT04261686
BARD® The VENOVO™ Venous Stent Study for Treatment of Iliofemoral Occlusive Disease
NCT02655887
Time and Motion Related to PICC Insertion Process and Catheter Tip Confirmation
NCT02498821
BARD® Study of LIFESTREAM™ Balloon Expandable Covered Stent Treating Iliac Arterial Occlusive Disease
NCT02228564
A Prospective, Multi-Center Study of Phasix™ Mesh for Ventral or Incisional Hernia Repair.
NCT01961687
Comparison of AccuCath IV Catheter and Conventional IV Catheter in Interventional Radiology
NCT01940354
Lutonix DCB Versus Standard Balloon Angioplasty for Treatment of Below-The-Knee (BTK) Arteries
NCT01870401
GalaFlex Mesh in Facelift
NCT02053831
FLUENCY® PLUS Endovascular Stent Graft for In-stent Restenosis
NCT01257438
A Retrospective Study With Prospective Follow-Up of Laparoscopic Ventral Hernia Repair Utilizing the Bard Sepramesh IP Composite
NCT01305473
Crosser Enters The Right Arterial Lumen
NCT01205386
Test for Pre Operative Skin Preparations
NCT00799812
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 3 | 1 |
Therapeutic Areas
What the Pipeline for C. R. Bard Shows
According to the ClinicalTrials.gov registry, C. R. Bard is linked to 46 US clinical trials across every stage of research activity. Of those, 32 studies are currently recruiting — about 70% of the sponsor's indexed portfolio — and 12 are already marked complete, representing roughly 26% of the total. Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.
The phase mix for C. R. Bard reports 1 late-stage studies (Phase 3 and Phase 4 combined) and 0 earlier-phase studies (Phase 1 and Phase 2). A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work — safety, dosing, and early signal detection — and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.
The top therapeutic focus area indexed for C. R. Bard is Arteriovenous Fistula with 3 linked trials, and 9 other condition areas appear in the top list above. That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice — verify current details directly with ClinicalTrials.gov before relying on any figure here.
Read our methodology — how this data is sourced, computed, and verified.