C. R. Bard

46 total trials 32 currently recruiting 12 completed

Trial Pipeline

RECRUITING NA

Real-World Registry of the Rotarex(TM) Rotational Excisional Atherectomy System (XTRACT Registry)

NCT07016698

RECRUITING NA

Study of GalaFLEX LITE™ Scaffold in Treatment of Capsular Contracture After Breast Implant Augmentation

NCT05945329

RECRUITING NA

Post-market Surveillance Study of the BD® WavelinQ™ EndoAVF System

NCT04634916

RECRUITING NA

Prophylactic Reinforcement of Ventral Abdominal Incisions Trial

NCT03911700

ACTIVE NOT RECRUITING NA

Venclose digiRF System Post Market Study

NCT05504070

ACTIVE NOT RECRUITING NA

Post Approval Study Investigating Lutonix Drug Coated Balloon for Treatment of Dysfunctional Arteriovenous Fistulae

NCT03506308

COMPLETED NA

Post Approval Study of the BARD® COVERA™ Arteriovenous (AV) Stent Graft

NCT04261686

COMPLETED NA

BARD® The VENOVO™ Venous Stent Study for Treatment of Iliofemoral Occlusive Disease

NCT02655887

COMPLETED NA

Time and Motion Related to PICC Insertion Process and Catheter Tip Confirmation

NCT02498821

COMPLETED NA

BARD® Study of LIFESTREAM™ Balloon Expandable Covered Stent Treating Iliac Arterial Occlusive Disease

NCT02228564

COMPLETED NA

A Prospective, Multi-Center Study of Phasix™ Mesh for Ventral or Incisional Hernia Repair.

NCT01961687

COMPLETED NA

Comparison of AccuCath IV Catheter and Conventional IV Catheter in Interventional Radiology

NCT01940354

COMPLETED NA

Lutonix DCB Versus Standard Balloon Angioplasty for Treatment of Below-The-Knee (BTK) Arteries

NCT01870401

COMPLETED

GalaFlex Mesh in Facelift

NCT02053831

COMPLETED NA

FLUENCY® PLUS Endovascular Stent Graft for In-stent Restenosis

NCT01257438

COMPLETED

A Retrospective Study With Prospective Follow-Up of Laparoscopic Ventral Hernia Repair Utilizing the Bard Sepramesh IP Composite

NCT01305473

COMPLETED

Crosser Enters The Right Arterial Lumen

NCT01205386

COMPLETED Phase 3

Test for Pre Operative Skin Preparations

NCT00799812

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.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial