C. R. Bard

Open enrollment with a later-stage pipeline tilt

According to ClinicalTrials.gov-derived indexes, C. R. Bard sits in the top decile of US sponsors by registered trial count (#290 of 15,742 sponsors by registered trial count).

75 total trials 4 currently recruiting 56 completed later-stage tilt top decile by trial count

C. R. Bard: 75 sponsored US clinical trials, 4 recruiting.

C. R. Bard sponsors 75 registered US clinical trials on ClinicalTrials.gov, 4 of them currently recruiting, and 56 completed. 10 of these trials are in Phase 3-4 (later-stage) and 4 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Arteriovenous Fistula, with 3 trials.

Top-decile sponsor footprint

C. R. Bard ranks in the top decile of sponsors by registered trial count (#290 of 15,742 sponsors by registered trial count). Volume at this scale usually reflects a long institutional pipeline, read phase tilt and therapeutic areas below before treating it as current-year activity.

Trial completion reliability score

F 42/100

56 of 69 decided trials (Completed vs. Terminated on ClinicalTrials.gov) reached their planned completion (81.2%), vs. national p10 68.4% / p90 100% among 1,234 sponsors with at least 10 decided trials. Still-open trials (Recruiting, Active-not-recruiting, Not-yet-recruiting) are excluded since they have not reached an outcome yet.

Open and recent trials

75 total, page 1 of 2

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

This Study Will Collect Clinical and Patient Reported Satisfaction Data From Males Requiring Urine Output Management Overnight in the Home Setting.

NCT06850259

COMPLETED NA

This Study Will Collect Clinical and Patient Reported Experience Data From Participants Requiring Urine Output Management Overnight in the Home Setting.

NCT06666426

COMPLETED NA

PureWick™ Adolescent Study

NCT06631313

COMPLETED NA

PureWick™ France and U.S. At-Home Pilot Study

NCT05710718

COMPLETED NA

Male External Catheters' Comparison of Comfort and Efficacy

NCT05955560

TERMINATED NA

The Pristine Post-Market Study

NCT05228132

COMPLETED NA

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

NCT04261686

COMPLETED NA

Caterpillar™ Arterial Embolization Device Post-Market Study

NCT04244370

COMPLETED

STARS-R Registry: Retrospective Analysis of Poly-4-hydroxybutyrate (P4HB) Scaffold Use

NCT04195854

TERMINATED NA

Lutonix Drug Coated Balloon for Treatment of Femoropopliteal Arteries in United States Females (CONFIRM)

NCT02813577

TERMINATED

SHERLOCK 3CG™ Diamond Tip Confirmation System

NCT03288766

COMPLETED

Real World Registry Assessing the Clinical Use of the Bard UltraScore Forced Focus PTA Balloon

NCT03193619

TERMINATED NA

Impact of Fever Prevention in Brain Injured Patients

NCT02996266

COMPLETED Phase 2

Evaluating Safety and Effectiveness of Octenidine Dihydrochloride

NCT03140254

COMPLETED NA

Clinical Study of the BARD® COVERA™ Arteriovenous (AV) Stent Graft in AV Graft Patients (AVeVA)

NCT02790606

COMPLETED NA

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

NCT02655887

COMPLETED NA

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

NCT02649946

COMPLETED NA

Safety and Effectiveness of a New Pleural Catheter for Symptomatic, Recurrent, MPEs Versus Approved Pleural Catheter

NCT02649894

COMPLETED NA

Xen Matrix™ AB Surgical Graft in Ventral or Incisional Midline Hernias

NCT02691962

COMPLETED NA

A Prospective Trial of a Bio-absorbable Mesh in Challenging Laparoscopic Ventral or Incisional Hernia Repair

NCT02712398

COMPLETED Phase 3

Study Comparing Lutonix AV Drug Coated Balloon vs Standard Balloon for Treatment of Dysfunctional AV Fistulae

NCT02440022

COMPLETED NA

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

NCT02498821

COMPLETED NA

Real-World Registry Assessing the Clinical Use of the Lutonix 035 Drug Coated Balloon Catheter

NCT02424383

COMPLETED NA

Prospective Feasibility Trial of AccuCath 2.25" Blood Control (BC) Placed in Difficult Access Patients in the Emergency Department

NCT02449798

COMPLETED NA

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

NCT02228564

COMPLETED NA

Lutonix® Drug Coated Balloon vs. Standard Balloon Angioplasty for Treatment of Femoropopliteal In-Stent Restenosis

NCT02063672

COMPLETED

Post-Marketing Study to Assess Complication Rates of Oncology Patients With Ports and Peripheral IVs

NCT02792764

COMPLETED NA

A Prospective, Multicenter All Comers Study of Phasix Mesh for Ventral or Incisional Hernia Repair

NCT02053168

COMPLETED NA

Progel Vascular Sealant

NCT01959503

COMPLETED

Study to Assess Electrocardiogram Waveforms Produced Through the Utilization of the Sherlock 3CG™ Tip Confirmation System

NCT03028090

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 NA

Progel® Pleural Air Leak Sealant (PALS) in Video and Robotic Assisted Thoracoscopic Surgery

NCT01867658

COMPLETED NA

AccuCath™ Intravenous (IV) Device Used by Vascular Access Team (VAT)

NCT01937195

COMPLETED NA

AccuCath Guidewire Intravenous (IV) Device Versus Conventional IV Catheter In General Nursing Use

NCT01943474

COMPLETED NA

LEVANT 2 Continuation Registry of the Lutonix® Drug Coated Balloon (DCB)

NCT01628159

TERMINATED

Study to Extend the Maximum Maintenance Flushing Interval for Ports With Distally Valved Catheters

NCT01586026

COMPLETED

GalaFlex Mesh in Facelift

NCT02053831

COMPLETED NA

LEVANT 2 Safety Registry

NCT01790243

COMPLETED NA

Moxy Drug Coated Balloon vs. Standard Balloon Angioplasty for the Treatment of Femoropopliteal Arteries

NCT01412541

COMPLETED NA

NeoMend ProGEL™ Pleural Air Leak Sealant Post-Approval Study

NCT01394978

COMPLETED NA

A Prospective, Multi-Center Study of the Bard® Denali™ Retrievable Inferior Vena Cava Filter System

NCT01305564

COMPLETED Phase 4

Topical Antimicrobial Effectiveness Testing

NCT01366417

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Where C. R. Bard enrollment is open (later-stage tilt)

4 recruiting of 75 indexed (5% open); 56 completed (75%).

Phase mix: 10 late (III/IV) vs 4 early (I/II) (later-stage heavy).

Top condition: Arteriovenous Fistula (3 trials), 9 others listed.

How open-pipeline share is computed

Recruiting share is recruiting_count divided by trial_count for this sponsor in the public registry export. Status can change between pulls; treat the figure as a research-attention snapshot, not product availability.

C. R. Bard: open-pipeline peers nationwide

Peers matched on 75 registered trials and 5% open enrollment, not the therapeutic-area sidebar.

C. R. Bard sits at or above the median trial volume and at or above the median recruiting share among these 9 nationwide peers -- the two do not always move together. Source: ClinicalTrials.gov (2026-08-08 snapshot). 2×2 strategic matrix plotting 9 entities by Total trials (X) and Recruiting share (Y), with a crosshair dividing the plot into four quadrants. Higher volume & more openFocused & more openHigher volume, mostly closedSmaller & mostly closed 020406080 0%10%20%30%40% Total trials Recruiting share C. R. BardECOG-ACRIN Cancer Research GroupHartford HospitalInova Health Care ServicesIonis PharmaceuticalsAlmirall, S.A.Cordis USDefense and Veterans Center for Integrative Pain ManagementDePuy Orthopaedics
C. R. Bard sits at or above the median trial volume and at or above the median recruiting share among these 9 nationwide peers -- the two do not always move together. Source: ClinicalTrials.gov (2026-08-08 snapshot).

C. R. Bard sits at or above the median trial volume and at or above the median recruiting share among these 9 nationwide peers -- the two do not always move together.

Sponsors near 75 trials (± recruiting share)

Sponsors near 5% open enrollment (± trial volume)

What to do with this C. R. Bard page

75 registered trials is a research-attention snapshot, not an endorsement of C. R. Bard or any single study.

  • 4 of C. R. Bard's trials are currently recruiting, check each one's own eligibility criteria before contacting a site. Browse recruiting trials
  • Arteriovenous Fistula is the condition C. R. Bard studies most, compare against other sponsors active in the same condition before evaluating a specific study. See Arteriovenous Fistula trials
  • Bring the specific trial ID (NCT number) to your own doctor before enrolling, this page is a directory, not medical guidance. Read the trial-finding guide

Trial and recruiting counts reflect ClinicalTrials.gov registry status as of the data vintage above; individual trial eligibility and enrollment status can change.

C. R. Bard pipeline card: 75 registered trials from official public datasets.Report a data error.