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NCT03561506

Effect of Preoperative Ferric Carboxymaltose After Simultaneous Bilateral Total Knee Arthroplasty

Status unknown Phase 4 Last updated 19 June 2018
What this trial tests

Phase 4 trial testing Ferric carboxymaltose in Postoperative Anemia in 80 participants. Status unknown.

Timeline
11 June 2018
Primary endpoint
11 June 2019
11 December 2019

Quick facts

Lead sponsorThe Catholic University of Korea
PhasePhase 4
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment80
Start date11 June 2018
Primary completion11 June 2019
Estimated completion11 December 2019

Drugs / interventions tested

Conditions studied

Sponsor

The Catholic University of Korea

Who can join

19 and older, any sex, with Postoperative Anemia or Knee Osteoarthritis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The primary purpose of this study is to evaluate the safety and efficacy of preoperative intravenous ferric carboxymaltose in patients with anemia undergoing Simultaneous Bilateral Total knee replacement in terms of Quality of life (QOL) and objective measures (Hb and Iron parameters).

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Ferric carboxymaltose

Trials testing the same drug.

Other The Catholic University of Korea trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03561506.

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