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Effect of Intravenous Ferric Carboxymaltose on Hemoglobin Response and Transfusion in Patients With Iron Deficiency Anemia After Off-Pump Coronary Artery Bypass Grafting

Primary Purpose

Coronary Artery Disease

Status
Unknown status
Phase
Phase 4
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Ferinject
Normal Saline Flush
Sponsored by
Yonsei University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronary Artery Disease focused on measuring Bleeding, Blood transfusion, Coronary artery bypass surgery, Hemostasis, Iron therapy

Eligibility Criteria

19 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. patients aged 19 years or older
  2. undergoing elective OPCAB or MIDCAB surgery with multi-vessel coronary artery disease.

Exclusion Criteria:

  1. Patients who underwent iron correction treatment (oral, injection, blood transfusion) within 2 months prior to surgery
  2. Patients taking anticoagulants before surgery
  3. Patients taking and administering drugs that can cause bone marrow suppression, such as anticancer drugs, before surgery
  4. Patients with chronic liver disease and chronic kidney disease undergoing dialysis
  5. Patients scheduled for coronary artery bypass graft for emergency surgery
  6. Patients with a history of hypersensitivity reactions and side effects to iron drugs
  7. Minor (under 20 years old)
  8. Definition of iron deficiency anemia (if all criteria a to c in the following items are satisfied)

    1. Ferritin<300mcg/L
    2. Transferrin saturation<25%
    3. Hb<12.0g/dL for women or Hb<13.0g/dL for men

Sites / Locations

  • Yonsei University Health System, Severance HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Ferinject®

Normal saline

Arm Description

Outcomes

Primary Outcome Measures

Total mediastinal blood loss and transfusion counts
For cost-effectiveness analysis of ferric carboxymaltose in preoperative iron treatment

Secondary Outcome Measures

blood loss in the operative day
amount of blood products transfused both intraoperatively and postoperatively
rate of surgical revision for bleeding
total length of intensive care unit (ICU) stay
rate of postoperative morbidity
rate of postoperative mortality

Full Information

First Posted
May 19, 2021
Last Updated
May 21, 2021
Sponsor
Yonsei University
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1. Study Identification

Unique Protocol Identification Number
NCT04898569
Brief Title
Effect of Intravenous Ferric Carboxymaltose on Hemoglobin Response and Transfusion in Patients With Iron Deficiency Anemia After Off-Pump Coronary Artery Bypass Grafting
Official Title
Effect of Intravenous Ferric Carboxymaltose on Hemoglobin Response and Transfusion in Patients With Iron Deficiency Anemia After Off-Pump Coronary Artery Bypass Grafting
Study Type
Interventional

2. Study Status

Record Verification Date
May 2021
Overall Recruitment Status
Unknown status
Study Start Date
February 10, 2019 (Actual)
Primary Completion Date
October 1, 2022 (Anticipated)
Study Completion Date
December 31, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Yonsei University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
In this prospective open-label randomized tral, 100 patients with elective off-pump coronary artery bypass (OPCAB) or minimal invasive direct coronary bypass (MIDCAB) surgery were enrolled. Before surgery, if a patient had iron deficiency anemia, the patient was randomized to receive Ferinject®(Ferric carboxymaltose, n=50) or placebo (normal saline, n=50), respectively. A single dose should not exceed 1000mg of iron per day or 20mg per kg body weight. In addition, the administration of 1000mg of iron should not exceed once a week. Administration to patients with hemodialysis-dependent chronic kidney disease is once daily, and the maximum dose should not exceed 200 mg (4 ml) of iron. Patients weighing less than 35 kg should not exceed 500 mg total iron dose. It uses intravenous infusion and can be administered up to 1,000mg (20ml) as the maximum iron once. For intravenous infusion, this drug is diluted with 0.9% sterile physiological saline solution.
Detailed Description
Perioperative blood loss and iatrogenic hemodilution lead to postoperative anemia which correlates with infections, and poor physical function, mobility and recovery with subsequent increases in the length of hospital stay and mortality. Preoperative anemia management reduce intraoperative blood loss such as normothermia, antifibrinolytics and cell salvage are key strategies to ameliorate postoperative anemia. Patient screening method Off-pump coronary artery bypass (OPCAB) under median-sternotomy, or minimal invasive direct coronary bypass (MIDCAB) undertaken under median-sternotomy Among them, the selection/exclusion criteria are checked and the subjects of the study are screened. * Inclusion/ exclusion criteria **Inclusion: Patients with Preoperative iron deficiency anemia Among Patients scheduled for cardiopulmonary coronary artery bypass graft under median sternotomy in cardiovascular surgery **Exclusion: - a) Patients who underwent iron correction treatment (oral, injection, blood transfusion) within 2 months prior to surgery b) Patients taking anticoagulants before surgery c) Patients taking and administering drugs that can cause bone marrow suppression, such as anticancer drugs, before surgery d) Patients with chronic liver disease and chronic kidney disease undergoing dialysis e) Patients scheduled for coronary artery bypass graft for emergency surgery f) Patients with a history of hypersensitivity reactions and side effects to iron drugs g) Minor (under 20 years old) 3) Definition of iron deficiency anemia (if all criteria a to c in the following items are satisfied) Ferritin<300mcg/L Transferrin saturation<25% Hb<12.0g/dL for women or Hb<13.0g/dL for men * The primary goal of this study was the effect of intravenous administration of ferric carboxymaltose on postoperative hemoglobin levels in patients with preoperative iron deficiency anemia among patients requiring cardiopulmonary coronary artery bypass grafting due to coronary artery disease. It is to analyze the effect compared to the control.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease
Keywords
Bleeding, Blood transfusion, Coronary artery bypass surgery, Hemostasis, Iron therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
In cardiac surgery, patients were randomized to receive Ferinject or placebo (n=50), respectively. The selected agent was intravenous infusion in general ward, preoperatively.
Masking
Participant
Masking Description
Patients were offered the allocated treatment for ferric carboxymaltose or not, using the block randomization system. The selected agent was infused to patients after randomization.
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Ferinject®
Arm Type
Experimental
Arm Title
Normal saline
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Ferinject
Other Intervention Name(s)
Colloidal solution of the iron complex ferric carboxymaltose
Intervention Description
Ferric carboxymaltose injection
Intervention Type
Drug
Intervention Name(s)
Normal Saline Flush
Other Intervention Name(s)
placebo comparator
Intervention Description
placebo
Primary Outcome Measure Information:
Title
Total mediastinal blood loss and transfusion counts
Description
For cost-effectiveness analysis of ferric carboxymaltose in preoperative iron treatment
Time Frame
At admission periods for Off-Pump Coronary Artery Bypass or Minimally Invasive Direct Coronary Artery Bypass surgery (Mean 8~9 days)
Secondary Outcome Measure Information:
Title
blood loss in the operative day
Time Frame
24 hours later after surgery
Title
amount of blood products transfused both intraoperatively and postoperatively
Time Frame
24 hours later after surgery
Title
rate of surgical revision for bleeding
Time Frame
intraoperative
Title
total length of intensive care unit (ICU) stay
Time Frame
mean 3-4 days
Title
rate of postoperative morbidity
Time Frame
Participants will be followed during 1 years from operation
Title
rate of postoperative mortality
Time Frame
Participants will be followed during 1 years from operation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients aged 19 years or older undergoing elective OPCAB or MIDCAB surgery with multi-vessel coronary artery disease. Exclusion Criteria: Patients who underwent iron correction treatment (oral, injection, blood transfusion) within 2 months prior to surgery Patients taking anticoagulants before surgery Patients taking and administering drugs that can cause bone marrow suppression, such as anticancer drugs, before surgery Patients with chronic liver disease and chronic kidney disease undergoing dialysis Patients scheduled for coronary artery bypass graft for emergency surgery Patients with a history of hypersensitivity reactions and side effects to iron drugs Minor (under 20 years old) Definition of iron deficiency anemia (if all criteria a to c in the following items are satisfied) Ferritin<300mcg/L Transferrin saturation<25% Hb<12.0g/dL for women or Hb<13.0g/dL for men
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Young-Nam Youn
Phone
82-10-9930-4522
Email
ysgs@yuhs.ac
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Young-Nam Youn
Organizational Affiliation
Division of Cardiovascular Surgery, Severance Cardiovascular Hospital, Yonsei University College of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Yonsei University Health System, Severance Hospital
City
Seoul
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Young-Nam Youn
Phone
82-10-9930-4522
Email
ysgs@yuhs.ac

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
31487129
Citation
Banerjee S, McCormack S. Intravenous Iron Preparations for Patients Undergoing Elective Surgery: A Review of Clinical Effectiveness, Cost-Effectiveness, and Guidelines [Internet]. Ottawa (ON): Canadian Agency for Drugs and Technologies in Health; 2019 Mar 27. Available from http://www.ncbi.nlm.nih.gov/books/NBK545893/
Results Reference
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Learn more about this trial

Effect of Intravenous Ferric Carboxymaltose on Hemoglobin Response and Transfusion in Patients With Iron Deficiency Anemia After Off-Pump Coronary Artery Bypass Grafting

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