Trial To Evaluate the Efficacy of Intravenous Iron in Older Adults With Unexplained Anemia

Duke University

Status and phase: Terminated; Phase 2

Conditions: Anemia; Unexplained Anemia (UAE)

Treatments: Drug: iron sucrose

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT01309659

U01AG034661 (U.S. NIH Grant/Contract)

Pro00028687

PACTTE_01

Details and patient eligibility

About

The purpose of this study is to determine whether treatment of unexplained anemia in older adults with a short course of weekly intravenous iron infusions can improve physical activity and therefore quality of life.

Full description

There is a tremendous morbidity and mortality associated with anemia in the elderly and the increasing proportion of elderly adults underscores the population's attributable risk of anemia. As a potentially modifiable factor, an urgent need exists to delineate the impact of anemia correction in the elderly. The Partnership for Anemia: Clinical and Translational Trials in the Elderly (PACTTE) consortium has been created to focus on treatment strategies for anemia in elderly patients. The data presented in this protocol provides a compelling rationale to evaluate the impact of a well-tolerated IV iron preparation in community dwelling older anemic adults with intermediate serum ferritin values.

Subjects will be 65 years or older adults with unexplained anemia and a serum ferritin between 20 and 200 ng/mL.

Subjects will be randomized on a 1:1 basis to either receive a 5 week course of treatment with intravenous iron immediately or to a waitlist control group who will receive treatment with intravenous iron following a 12 week observation period. Both groups will ultimately receive 200mg of intravenous iron sucrose weekly for 5 weeks to determine if this can lead to improvement in 6 Minute Walk Test results. The primary endpoint is change in 6 Minute Walk Test distances from baseline to 12 weeks. The procedures in this protocol will include the use of outcomes tools that have been selected for their ability to show improvement in quality of life in this patient population. Blood samples will also be collected for analysis both at the local lab (safety tests - eg hemoglobin or Hb) or at a central lab for research purposes.

Enrollment: 19 patients

Sex: All

Ages: 65+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age ≥ 65 years old
• Hemoglobin concentration ≥ 9.0 g/dL and < 11.5 g/dL (women) or < 12.7 g/dL (men)
• Unexplained anemia
• Serum ferritin level ≥ 20 and ≤ 200 ng/mL
• Able to walk without the use of a walker, motorized device or the assistance of another person.
• Able to understand and willing to provide written informed consent in the absence of dementia
• Must be able to understand and speak in English

Exclusion criteria

• Red blood cell transfusions within the past 3 months
• Use of erythropoiesis stimulating agents (ESA) in the past 3 months
• Intravenous Iron Infusions within the past 3 months
• Distance on baseline 6MWT (6 minute walk test) above the median for age and sex
• History of unstable angina or myocardial infarction in the past 3 months
• History of stroke or TIA (transient ischemic attack) the past 3 months
• Uncontrolled hypertension (diastolic blood pressure > 100 mm Hg or systolic blood pressure > 160 mm Hg on 2 separate occasions)
• Positive fecal occult blood test within the screening period
• Elevated AST (aspartate aminotransferase) or ALT (alanine aminotransferase) ≥ 2x upper limit of normal
• Documented anaphylactic reaction to iron sucrose infusion in the past
• Subjects initiated on oral iron supplementation within the last 6 weeks, or those initiated on oral iron within the last 3 months who have had at least a one gram/dL improvement in Hb since starting oral iron supplementation

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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19 participants in 2 patient groups

Immediate Intervention Group

Experimental group

Description:

Subjects randomized to the immediate treatment group will be scheduled to begin treatment with IV iron infusion immediately (or within 2 business days). They will receive 200mg IV iron sucrose a week for 5 weeks followed by 19 weeks of follow up.

Treatment:

Drug: iron sucrose

Drug: iron sucrose

Wait List Control

Experimental group

Description:

Subjects randomized to the wait list control group will have an observation visit at week 6 and week 12. After that they will begin treatment with IV iron infusion. They will receive 200mg IV iron sucrose a week for 5 weeks followed by 7 weeks of follow up

Treatment:

Drug: iron sucrose

Drug: iron sucrose