Skåne University Hospital
Malmö, Sweden
NCT Number: NCT06121115
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
Looking for future studies?
Notify Me18 year and older
All sexes
Observational
Malmö, Sweden
Se attached study protocol
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Norepinephrine administered in midline catheter according to clinical routine
Other names: Vasopressors
Time frame: day 30
extravasation of norepinephrine, midline-associated bloodstream infection, thrombosis
Time frame: day 30
infiltration, occlusion of midline, dislodgement, leakage, other
Time frame: day 30
Has the patient received central line after midline placement
Time frame: day 30
Where did the patient go after intermediary care? discharged / escalated to the ICU / deceased
Region Skane
Other
Norepinephrine Administration Through a Midline Catheter in an Intermediate Care Unit - a Retrospective Study of Complications and Patient Outcomes
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07039227
Cardiovascular Diseases, Embolism and Thrombosis
Rouen, France
View Trial DetailsNCT05630716
Cardiovascular Diseases, Hypotension
Minneapolis, Minnesota, United States
View Trial DetailsNCT06181604
Infections, Inflammation
Boston, Massachusetts, United States
View Trial DetailsNCT02473718
Cardiovascular Diseases, Fluid Therapy
View Trial Details