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NCT06037525 Clinical Trial

Clinical Evaluation of the PowerGlide™ Pro Midline Catheter

Pain Clinical Trial

— Midline  

Official title:
Clinical Evaluation of the PowerGlide™ Pro Midline Catheter

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06037525
Other study ID # MIDLINE
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2018
Est. completion date May 1, 2023

Study information
Verified date November 2023
Source University Hospital Augsburg
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Clinical evaluation of the PowerGlide™ Pro Midline Catheter in patients with vascular diseases

Description:

Clinical evaluation of the PowerGlide™ Pro Midline Catheter in patients with vascular diseases. The selected patients are in need of a long-term i.v. therapy for reasons as antibiotic therapy or alprostadil therapy. The Midline catheter is a device, which is placed via Seldinger's technique to a vein usual on the upper extremity under ultrasound-control.

Recruitment information / eligibility
Status Completed
Enrollment 50
Est. completion date May 1, 2023
Est. primary completion date November 13, 2020
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - need for i.v. therapy longer than 7 days - poor peripheral vein status - Administration of alprostadil Exclusion Criteria: - pending dialysis - allergy to catheter material - minor age - life threatening conditions - requirement for central venous catheter

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• PowerGlide™ Pro Midline Catheter
Clinical evaluation of the PowerGlide™ Pro Midline Catheter in patients with vascular disease

Locations
Country Name City State
Germany University Hospital Augsburg Augsburg

Sponsors (1)
Lead Sponsor Collaborator
University Hospital Augsburg

Country where clinical trial is conducted

Germany, 

Outcome
Type Measure Description Time frame Safety issue
Primary Dwelling Time Length of catheter in situ time 0-29 days
Secondary Administration of Alprostadil Feasibility for the usage of Alprostadil measured by patients with development of thrombophlebitis or occlusion 0-29 days
Secondary Catheter Complications Site complications as thrombophlebitis and occlusion 0-29 days
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