Characteristics of Patients With Hypersensitivity Reactions to Intravenous Iron Infusions

University Hospital Basel

Status: Completed

Conditions: Iron-deficiency; Hypersensitivity Reactions

Treatments: Other: collection of patient data

Study type: Observational

Funder types: Other

Identifiers

NCT04359368

2019-01266 sp20Steveling3;

Details and patient eligibility

About

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.

Enrollment: 42 patients

Sex: All

Ages: 16+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Participants from 16 years of age and older with previous hypersensitivity reaction grades I-IV to intravenous ferric carboxymaltose (Ferinject) or to iron sucrose (Venofer).

Exclusion criteria

• No previous hypersensitivity reaction to iron preparations or reactions to oral iron preparations.
• If a rejection to use patient data is documented in patient records, the patient will be excluded from analysis.

Trial design

42 participants in 1 patient group

patients with hypersensitivity reactions to NDIPs

Description:

Patients with previous hypersensitivity reaction grades I-IV to intravenous ferric carboxymaltose (Ferinject) or to iron sucrose (Venofer)

Treatment:

Other: collection of patient data