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B.D Accucath 5.71 cm 20 Gauge ultralong intravenous catheter for Peripheral Intravenous Catheter Phlebitis
N/A
Waitlist Available
Led By Amit Bahl, MD.
Research Sponsored by William Beaumont Hospitals
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up study period, a maximum of 1 year
Awards & highlights
Study Summary
This trial is testing whether a new type of IV catheter is just as good as the old one.
Eligible Conditions
- Peripheral Intravenous Vein Catheter Phlebitis
- Intravenous Infection
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ study period, a maximum of 1 year
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~study period, a maximum of 1 year
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Catheter survival
Secondary outcome measures
Catheter-associated bloodstream infection
Catheter-associated thrombosis
First-stick success.
+3 moreOther outcome measures
Inflammatory complications by clinical assessment
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Experimental Arm B.D. Accucath 5.71 cm 20 Gauge catheterExperimental Treatment1 Intervention
Device BD 5.71 cm Accucath IV catheter with guidewire
Group II: Control Arm B.Braun 6.35 cm 20 Gauge catheterActive Control1 Intervention
Device 6.35 cm 20 Gauge B. Braun catheter without guidewire
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Who is running the clinical trial?
William Beaumont HospitalsLead Sponsor
149 Previous Clinical Trials
112,858 Total Patients Enrolled
Amit Bahl, MD.Principal InvestigatorWilliam Beaumont Hospitals
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- The person performing the ultrasound guided IV insertion should have at least 6 months of experience.You can't fully move your elbow.You have difficulties with thinking, understanding, or remembering things.
Research Study Groups:
This trial has the following groups:- Group 1: Control Arm B.Braun 6.35 cm 20 Gauge catheter
- Group 2: Experimental Arm B.D. Accucath 5.71 cm 20 Gauge catheter
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
What is the current participant count of this clinical trial?
"Affirmative. Clinicaltrials.gov has data that shows the recruitment for this medical trial, which was first posted on December 1st 2023, is still ongoing. A total of 370 patients are expected to be enrolled from a single clinical site."
Answered by AI
Is the trial currently open for enrollment?
"Affirmative. Evidenced by the information posted on clinicaltrials.gov, this medical trial is still recruiting patients who meet its criteria; it was first published in December 1st 2023 and most recent modified in October 28th 2022. Currently, 370 individuals are needed from one clinic site."
Answered by AI
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