Status:
COMPLETED
Peripheral Intravenous Catheter Securement With Tissue Adhesive
Lead Sponsor:
Corewell Health East
Conditions:
Vascular Access Devices
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
This clinical trial will compare survival of peripheral intravenous (IV) catheters for patients with a standard IV site dressing alone to patients with standard IV dressing plus Adhezion Biomedical Se...
Detailed Description
Patients admitted from the Emergency Department (ED) to a progressive floor, or patients admitted from ED to any floor type with express approval from the Principal Investigator are eligible participa...
Eligibility Criteria
Inclusion
- Greater or equal to 18 years of age
- Admission from the Emergency Department (ED) to a progressive floor, or Admission from ED to any floor type with express approval from the Principal Investigator
- IV placement in the antecubital fossa, forearm, wrist or hand
- IV placement in the ED
- Enrollment within 8 hours of IV insertion
- 18 or 20 gauge 1.16 inch IV catheter
- Expected hospital admission \>48 hours
Exclusion
- Patients with ultrasound-guided IV insertions
- Alternate site of cannulation
- Voluntary withdrawal
- Patients with a non-standard polyurethane dressing
- Known allergy to cyanoacrylate or formaldehyde
Key Trial Info
Start Date :
September 16 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 10 2020
Estimated Enrollment :
350 Patients enrolled
Trial Details
Trial ID
NCT04086693
Start Date
September 16 2019
End Date
October 10 2020
Last Update
December 6 2021
Active Locations (1)
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1
Beaumont Health System
Royal Oak, Michigan, United States, 48073