The effect of intravenous iron on postoperative transfusion requirements in hip fracture patients - the IVANOF1 Study

Not Applicable

Completed

• Conditions: Blood, Injuries and Emergencies; Surgery; Presence of orthopaedic joint implants

• Registration Number: ISRCTN76424792
• Lead Sponsor: niversity of Nottingham (UK)

Brief Summary

2013 protocol in: http://www.ncbi.nlm.nih.gov/pubmed/24015990 2019 results in: https://www.ncbi.nlm.nih.gov/pubmed/31127269 (added 29/05/2019)

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2012-09-10
• Study Completion: 2014-03-12
• Last Update Posted: 26 June 2019

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 80

Inclusion Criteria

1. Primary hip fracture
2. Aged over 70
3. Able to consent for themselves
4. Male and female participants

Exclusion Criteria

1. Undisplaced intracapsular fractures (very low transfusion requirements
2. Contraindications to intravenous iron
3. Currently taking antiplatelet drugs other than aspirin

Study & Design

• Study Type: Interventional
• Study Design: Not specified