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NCT06121115 Clinical Trial

Norepinephrine Administration Through a Midline Catheter in an Intermediate Care Unit

Septic Shock Clinical Trial

Official title:
Norepinephrine Administration Through a Midline Catheter in an Intermediate Care Unit - a Retrospective Study of Complications and Patient Outcomes

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06121115
Other study ID # 2022-06476
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 3, 2023
Est. completion date March 1, 2024

Study information
Verified date March 2024
Source Region Skane
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is a single-center study retrospectively evaluating a local clinical routine to administer norepinephrine in midline catheters, with regard to complications and patient outcomes

Description:

Se attached study protocol

Recruitment information / eligibility
Status Completed
Enrollment 473
Est. completion date March 1, 2024
Est. primary completion date March 1, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Administration of norepinephrine in a midline catheter in an intermediary care unit - In Skåne university hospital - From 2019 to 2023-03-31 Exclusion Criteria: - Patients who have actively disabled review of their electronic medical record

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Norepinephrine
Norepinephrine administered in midline catheter according to clinical routine

Locations
Country Name City State
Sweden Skåne University Hospital Malmö

Sponsors (1)
Lead Sponsor Collaborator
Region Skane

Country where clinical trial is conducted

Sweden, 

Outcome
Type Measure Description Time frame Safety issue
Primary Proportion of patients with a major complication of norepinephrine administration in midline extravasation of norepinephrine, midline-associated bloodstream infection, thrombosis day 30
Secondary Proportion of patients with a minor complication of norepinephrine administration in midline infiltration, occlusion of midline, dislodgement, leakage, other day 30
Secondary Proportion of patients receiving a CVC after midline Has the patient received central line after midline placement day 30
Secondary Proportion of patients with different intermediary care unit outcomes Where did the patient go after intermediary care? discharged / escalated to the ICU / deceased day 30
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