Effects of Oral Iron on Postoperative Fatigue Upon Coronary Artery Bypass Graft Patients

Phase III Randomized Double Blind Placebo-Controlled Study To Assess The Effects Of FeraMax When Administered Orally Once A Day On Postoperative Fatigue Levels In Patients Following Elective Coronary Artery Bypass Graft Surgery (CABG)

The purpose of this research study is to examine how an oral iron supplement (Feramax®) influences fatigue during early postoperative recovery (at three months) among CABG patients and, the effects on recovery outcomes (e.g. quality of life, functional capacity, anemia, and medication adherence).

It is hypothesized that CABG surgery patients receiving oral iron (Feramax®) 150mg orally (once a day therapy) will have a 15% reduction in POF (measured by the Identity Consequence Fatigue Scale (ICFS)), compared to patients receiving a placebo.

Study Overview

• Status: Terminated
• Conditions: Fatigue
• Intervention / Treatment: Drug: Polysaccharide iron complex; Drug: Placebo

Detailed Description

Postoperative fatigue (POF) is one of the main complaints in approximately 39-80% of CABG surgery patients. POF can have a significant impact on an individual's quality of life (QoL) and recovery. The objectives are to examine how an oral iron (Feramax®) influences fatigue during early postoperative recovery (at three months) among CABG patients and determine the effects on recovery outcomes (e.g. QoL, functional capacity, anemia, and medication adherence). To achieve these objectives the research will aim to answer the following questions:

1. Is oral iron effective in reducing POF measured by the Identity Consequence Fatigue Scale (ICFS) over 12 weeks?
2. If oral iron is effective, how effective was it on improving fatigue, functional capacity, QoL, and anemia?
3. To what degree do patients taking oral iron adhere to the prescription? A prospective, randomized, double-blind placebo-controlled, single-center study was chosen for this study. Three hundred participants who are scheduled for an isolated CABG surgery will be recruited from the QEII Health Sciences Centre (QEIIHSC), Halifax, Nova Scotia. All study participants will be followed for three months following hospital discharge.

Data will be collected at five time points:

Time point 1 Baseline -Patients are screened in the preadmission clinic or nursing unit and recruited for the study. During this visit, the patient will be assessed for eligibility, demographic data and blood work collected and three questionnaires and six minute walk test completed by participants.

Time point 2 Discharge/Randomization-Patients will be randomized to either FeraMAX® or placebo at hospital discharge. The treatment will be taken once daily for 84 days starting Day 1 (day after discharge from hospital). The questionnaires, six minute walk test and blood work will be repeated.

Time point 3 -Post testing 7 to 14 days post discharge A follow up telephone call to reminder patients to take medications and fill put side effects diary

Time Point 4 Six week Follow up-Blood work will be collected and three questionnaires and six minute walk test completed by participants.

Time Point 5-End of treatment-The questionnaires, six minute walk test, blood work, collect side effects diary and pill count will be repeated during a clinic visit.

Fatigue will be measured with the ICFS and Functional Assessment of Cancer Therapy Anemia( FACT-An) questionnaire. The Short Form-36 is used to measure QoL and the six minute walk test to measure functional capacity. Standard of care laboratory tests including (hemoglobin (Hgb) level, reticulocyte count, ferritin, iron, total iron binding capacity (TIBC), transferrin saturation, and C-Reactive Protein levels will be drawn. Medication adherence to the will be assessed by pill count.

The primary endpoint will be analyzed using ANOVA for repeated measures to compare level of fatigue of two groups at baseline, discharge, six weeks and 12 weeks. For the secondary endpoint, a subgroup analysis will be performed and reported on participants with and without iron- deficiency anemia to determine if any efficacy of iron on POF is restricted to this population or to a more general population post CABG surgery. Results will be reported using mean and standard deviation when appropriate and median (interquartile range) for nonparametric data. Categorical variables will be compared using Fisher exact test or t test when appropriate. Level of significance was set at p < 0.05.

Oral iron is inexpensive and effective treatment for iron deficiency that occurs from surgical blood loss. Currently there is no specific drug used to treat POF. Standard of care for POF consists of treating and eliminating the underlying symptoms.

• Study Type: Interventional
• Enrollment (Actual): 121
• Phase: Phase 3

Contacts and Locations

Study Locations

• Canada
  • Nova Scotia
    • Halifax, Nova Scotia, Canada, B3H3A7
      • Capital Health

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 19 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Non-Urgent, first time, coronary artery bypass grafting.

• American Society of Anesthesia (ASA) physical status II-IV
• Aged 19 years and older
• Able to make informed consent by understanding the nature of the participation
• Able to read and write English to the degree necessary to participate in interviews and questionnaires

Exclusion Criteria:

• Had prior median sternotomy surgery
• A Hemoglobin greater than or equal 120g/L at discharge
• Previous history of noncompliance with oral medications
• Received erythropoiesis-stimulating agents (e.g. epoetin alfa and darbepoetin alfa) postoperatively to discharge
• Allergy to iron History of hematological disorders that are deemed clinically significant as per the investigator's clinical judgment
• Received Clopidogrel within two days prior to surgery, greater than 81mg of Acetylsalicylic acid 24 hours prior to surgery, or have received "new oral anticoagulants" (e.g. Apixaban, Rivaroxaban, and Dabigatran) within the recommended preoperative exclusion period
• History of iron metabolism disorders e.g. known iron overload, hemochromatosis, porphyria
• Chronic fatigue syndrome (a condition that is distinguished from other types of fatigue by fatigue lasting more than six months and has at least four other symptoms (e.g. sleep disturbances, headaches, joint pain, and concentration difficulties) that could contribute to increased fatigue (Afari & Buchwald, 2003)).
• A serum transferrin saturation of more than 50% at discharge
• History of Fibromyalgia
• Current diagnosis of depressive disorder
• History of Hypothyroidism includes uncontrolled thyroid disease (abnormal Thyroid Stimulating Hormone (TSH) or Thyroxine (T4) at screening visit) as per the Investigator's clinical judgment
• Patient taking iron supplementation ≤ 60 days before surgery and in the postoperative period
• Any other unstable conditions as per the Investigator's clinical judgment
• Contraindications to the six-minute walk test
• Physical disability preventing safe performance
• Resting heart rate > 120 beats/min 10 min after rest (relative contraindications)
• Systolic blood pressure >180mm ± Diastolic blood pressure > 100mm Hg (relative contraindications)
• Resting Sp02 <85% on room air or on a prescribed level of supplemental oxygen

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Triple

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: FeraMax; FeraMax Polysaccharide iron complex oral iron supplement 150mg one capsule orally daily	Drug: Polysaccharide iron complex; 150 mg daily orally times 84 days; Other Names: FeraMAX
Placebo Comparator: Placebo; one capsule orally daily	Drug: Placebo; one capsule orally daily times 84 days; Other Names: Sugar pill

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Fatigue Level	Identity Consequence Fatigue scale	12 weeks after surgery

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Health Related Quality of Life	Self Report Scale Medical Outcomes Study short Form 36 to measure Quality of Life	12 weeks after discharge from hospital
Anemia	Functional Assessment of Cancer Therapy - Anemia Version 4 and Hemoglobin levels	12 week after surgery
Functional Capacity	Six Minute Walk Test	12 weeks after surgery
Medication Adherence	Pill Count	12 weeks after surgery

Collaborators and Investigators

• Sponsor: Nova Scotia Health Authority
• Collaborators: Dalhousie University; Capital Health, Canada
• Investigators: Principal Investigator: Blaine Kent, MD, Capital Health, Canada

Study record dates

Study Major Dates

• Study Start (Actual): December 16, 2014
• Primary Completion (Actual): February 21, 2018
• Study Completion (Actual): February 1, 2019

Study Registration Dates

• First Submitted: July 29, 2013
• First Submitted That Met QC Criteria: July 29, 2013
• First Posted (Estimate): July 31, 2013

Study Record Updates

• Last Update Posted (Actual): July 26, 2019
• Last Update Submitted That Met QC Criteria: July 24, 2019
• Last Verified: July 1, 2019

More Information

Terms related to this study

• Keywords: Adherence; Quality of Life; Anemia; Iron; Coronary artery bypass grafting; Postoperative fatigue; Functional Capacity
• Additional Relevant MeSH Terms: Fatigue
• Other Study ID Numbers: TheEffectsofOral Iron052013

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: No