Status:
UNKNOWN
Intraoperative IV Iron on Postoperative Red Blood Cell Recovery
Lead Sponsor:
Konkuk University Medical Center
Conditions:
Osteoarthritis, Hip
Eligibility:
All Genders
20-80 years
Phase:
PHASE4
Brief Summary
The objective of the present study is to determine the impact of intraoperative IV-iron supplementation on postoperative recovery of RBC mass by retrospectively analyzing and comparing the changes of ...
Eligibility Criteria
Inclusion
- Inclusion criteria
- Patients with osteoarthritis in knee joint undergoing elective uni-limb total knee arthroplasty surgery
- Patients provided a written informed consent.
- Patients with s-ferritin \< 300 mg/dl (male) or 200 mg/dl (female)
- Patients with preoperative serum hemoglobin concentration \>10 g/dL
- Exclusion criteria
- Patients with history of anaphylaxis, iron overload, active infection.
- Patients received or receiving intraoperative and preoperative blood salvaged, allogenic blood transfusion, recombinant human erythropoietin, or undergoing acute normovolemic hemodilution.
Exclusion
Key Trial Info
Start Date :
March 1 2021
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2021
Estimated Enrollment :
46 Patients enrolled
Trial Details
Trial ID
NCT04035902
Start Date
March 1 2021
End Date
December 1 2021
Last Update
August 19 2020
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