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Effect of intravenous iron supplementation in two-stage revision surgery of hip and knee arthroplasty

Effect of intravenous iron supplementation in two-stage revision surgery of hip and knee arthroplasty - Iron suppplementation in two-stage revisions

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00026116
Enrollment
40
Registered
2021-09-24
Start date
2021-10-01
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

D62

Interventions

Group 1: Anaemic patients (male hb <13g/dl, female hb < 12 g/dl) who underwent the first stage of a two stage revision of their hip or knee prosthesie and who received an intravenous iron supplementat

Sponsors

Orthopädische Klinik König-Ludwig-Haus
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Group 1 (intervention): - hip or knee prosthesis explanted and replaced by spacer, - scheduled for re-implantation, - intravenous iron administration during the interval after explantation and before re-implantation, - no clinical signs of persistent infection at the time point of iron administration Group 2 (historic control): - prosthesis explanted and replaced by spacer, - scheduled for re-implantation, matched pair for group 1 according to type of joint, age, ASA score, gender and severeness of anaemia at the time point of iron supplementation

Exclusion criteria

Exclusion criteria: Group 1: none. Group 2: intravenous iron administration, - persistent clinical signs of infection at the matched patient's time point of iron administration

Design outcomes

Primary

MeasureTime frame
Transfusion of allogenic red blood cells during or shortly after the re-implantation of the prosthesis.

Secondary

MeasureTime frame
Occurrence of adverse events after iron administration; mobility and length of stay after second surgery.

Countries

Germany

Contacts

Public ContactAxel Jakuscheit

Orthopädische Klinik König-Ludwig-Haus

a-jakuscheit.klh@uni-wuerzburg.de0049 931 803 0

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026