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 anaemiaIntravenous 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 anaemiaAnaesthesiology - Other anaesthesiologyBlood - AnaemiaMental 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
Name Time Method 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
Name Time Method 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]