Clinical Trials Directory

Trials / Completed

CompletedNCT04359368

Characteristics of Patients With Hypersensitivity Reactions to Intravenous Iron Infusions

Characteristics of Patients With Hypersensitivity Reactions to Intravenous Iron Infusions - a Retrospective Study

Status
Completed
Phase
Study type
Observational
Enrollment
42 (actual)
Sponsor
University Hospital, Basel, Switzerland · Academic / Other
Sex
All
Age
16 Years
Healthy volunteers
Not accepted

Summary

This study aims to evaluate characteristics of patients with previous hypersensitivity reaction grades I-IV to intravenous ferric carboxymaltose (Ferinject) or to iron sucrose (Venofer) including age, atopy status, previous allergic reactions, previous medical history, current medications and co-morbidities. Furthermore, symptoms on reaction such as severity grade of reaction will be evaluated.

Conditions

Interventions

TypeNameDescription
OTHERcollection of patient dataData collection (history, clinical presentation, medication, complications, laboratory testing) will be performed from patient records stored in the protected electronic patient system ISMed (Integrated System for Medical Diagnostic) of patients with HSRs to NDIPs.

Timeline

Start date
2019-09-01
Primary completion
2019-10-31
Completion
2019-10-31
First posted
2020-04-24
Last updated
2020-04-24

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT04359368. Inclusion in this directory is not an endorsement.