Overview

Intravenous Iron Sucrose in Arthroplasty

Status:
Unknown status
Trial end date:
2016-09-01
Target enrollment:
0
Participant gender:
All
Summary
The objective of the present study is to determine the impact of intraoperative IV-iron supplementation on postoperative oxygenation profile by comparing the postoperative PaO2/FiO2 ratio with or without IV-iron supplementation in old patients undergoing elective uni-limb arthroplasty surgery.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Konkuk University Medical Center
Treatments:
Ferric Compounds
Ferric Oxide, Saccharated
Iron
Criteria
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 >13 g/dL (male) and >12 g/dL
(female)

- Patients with PaO2/FiO2 ratio >150

Exclusion Criteria:

- Patients with history of anaphylaxis, iron overload, active infection.

- Patients with endocrine disease

- Patients received or receiving intraoperative and preoperative blood salvaged,
allogenic blood transfusion, anti-fibrinolytic agents or recombinant human
erythropoietin, or undergoing acute normovolemic hemodilution.