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The effect of different preparation information on side effects following intravenous iron infusio

Completed
Conditions
Intravenous iron infusion-Indicated for patients with iron deficiency anaemia for whom oral iron is considered considered unsuitable or has been unsuccessfule.g. due to malabsorption, continuing blood loss, poor adherence or intolerance to oral iron, preoperative iron deficiency anaemia
Intravenous iron infusion
-Indicated for patients with iron deficiency anaemia for whom oral iron is considered considered unsuitable or has been unsuccessful
e.g. due to malabsorption, continuing blood loss, poor adherence or intolerance to oral iron, preoperative iron deficiency anaemia
Anaesthesiology - Other anaesthesiology
Blood - Anaemia
Mental Health - Studies of normal psychology, cognitive function and behaviour
Registration Number
ACTRN12616001415493
Lead Sponsor
Keith Petrie
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
86
Inclusion Criteria

To be eligible to participate in the trial, individuals must:
-be over 18 years of age
-be a patient referred to the Auckland City Hospital Anaesthesia Department for an IV iron infusion

Exclusion Criteria

Individuals will not be eligible to participate in this study if they:
-are unable to give informed consent
-are unable to speak, write and read English

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Side effect reporting<br><br>Side effects will be assessed by self-report on a (study-designed) questionnaire. The participant will complete this questionnaire.[Immediately after IV Iron infusion]
Secondary Outcome Measures
NameTimeMethod
side effect reporting[3 days after IV iron infusion<br><br>Side effects will be assessed by self-report on a (study-designed) questionnaire. This questionnaire will be administered over telephone by the research assistant]
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