Peripheral Intravenous Catheter Securement With Tissue Adhesive
Completed · Not applicable
Conditions studied: Vascular Access Devices
In brief
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 SecurePortIV Catheter Securement Adhesive. Emergency room patients who already have IVs may be considered for inclusion. Eligible patients will be approached and, if they are interested in participating, their informed consent will be obtained. Participation will continue for up to 7 days. During this time, the patient will experience: * Assessment of their currently placed peripheral IV catheter, to assess if it is functioning * Assignment to one of two study groups (standard IV dressing or standard IV dressing plus Adhezion Biomedical SecurePortIV Catheter Securement Adhesive). This is called randomization and group assignment is by chance, like the flip of a coin * Daily assessment of the IV catheter and site for complications (such as infection or phlebitis), removal, and medications being administered.
Key facts
- Study ID
- NCT04086693
- Run by
- Corewell Health East
- People needed
- 350
- Starts
- 2019-09-16
- Expected to finish
- 2020-10-10
- Last updated by the study team
- 2021-12-06
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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
You may not qualify if…
- 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
Where it is running
- Beaumont Health System — Royal Oak, Michigan, United States
Full record on ClinicalTrials.gov
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