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Completed

NCT Number: NCT03106298

Iron Deficiency and FGF23 Regulation in CKD and HF

This study investigates the effects of intravenous (IV) iron sucrose therapy on blood levels of Fibroblast Growth Factor 23 (FGF23, a protein that regulates the amount of phosphate in the body) in iron deficiency anemia in healthy participants, participants with Congestive Heart Failure (CHF, where the heart does not pump adequate blood supply to the body), participants with Chronic Kidney Disease (CKD, where the kidney function is reduced), and participants with CKD and CHF.

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Key information

About this study

Iron is a key part of our red blood cells which bring oxygen to our body's tissues. Without iron, our blood cannot carry oxygen. The body normally gets iron through diet and it also re-uses iron from old red blood cells. When iron stores are low, patients get iron deficiency anemia. This can happen because patients lose more red blood cells and iron than the body can replace, the body does not do a good job at absorbing iron from the diet, or the body is able to absorb iron but patients are not getting enough iron from their diets. Many patients with chronic diseases such as CKD and CHF also have iron deficiency anemia.

Iron deficiency may also cause a hormone in the body named FGF23 to rise. FGF23 is a hormone that is made in bone and has an important role in the heart and kidney. When the kidneys are not working properly, as in CKD, or when the heart is not pumping correctly, as in CHF, FGF23 levels in the blood go up. Many patients with CKD or CHF also have low levels of iron. In these cases, FGF23 levels may rise even more. Too much FGF23 in the blood may lead to an increased risk of heart problems and accelerate loss of kidney function. The best way to control FGF23 levels in the blood in CKD and CHF is not known.

The investigators are conducting a 6-week iron deficiency anemia study on healthy individuals,individuals with CKD, and individuals with CHF to find out if treating iron deficiency anemia with intravenous iron sucrose therapy can safely and successfully lower FGF23 levels. Iron sucrose has been shown to lower FGF23 in animal models. The short term effects of iron sucrose on FGF23 levels in CKD and CHF are not known.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 18 years old
  • Ability to understand and the willingness to sign a written informed consent.
  • Iron Deficiency Anemia, as defined by
  • Ferritin level < 100 ng/ml or
  • Transferrin saturation <20% with ferritin 100-350 ng/ml and
  • Hemoglobin < 12 g/dl

Exclusion criteria

  • Hypersensitivity to any component of iron sucrose
  • Malignancy within 5 years
  • End stage renal disease or kidney transplantation
  • Erythropoiesis stimulating agents
  • Red blood cell transfusions within last 60 days
  • Current radiotherapy or chemotherapy
  • Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) levels greater than 1.5 times normal
  • Hemochromatosis
  • Chronic digestive diseases
  • Pregnancy or nursing
  • Active alcohol or drug abuse
  • Uncontrolled hypertension
  • Active infection
  • Hospitalization in the 4 preceding weeks
  • Concomitant use of antibiotics
  • Concomitant use of immunosuppression
  • Inability to consent.
  • Conditions, in which of the opinion of the investigator, make participation unacceptable

Treatment and study plan

Iron sucrose

Drug

All participants will be given intravenous iron sucrose (200 mg) weekly for 5 weeks. Iron sucrose is infused over 60 minutes.

Other names: Venofer

Primary outcomes

  1. Change in c-terminal FGF23 measurements

    Time frame: Weekly x 6 weeks, 1 longitudinal measurement at 3 months

    longitudinal change in plasma c-terminal FGF23 (RU/ml) over 6 weeks and 3 months

  2. Change in Intact FGF23 measurements

    Time frame: Weekly x 6 weeks, 1 longitudinal measurement at 3 months

    longitudinal change in plasma intact FGF23 (pg/ml) over 6 weeks and 3 months

Secondary outcomes

  1. Change in Parathyroid Hormone

    Time frame: Weekly x 6 weeks, 1 longitudinal measurement at 3 months

    longitudinal change in Serum Parathyroid Hormone (pg/ml) over 6 weeks and 3 months

  2. Change in Phosphate (mg/dl)

    Time frame: Weekly x 6 weeks, 1 longitudinal measurement at 3 months

    longitudinal change in Plasma Phosphate (mg/dl) over 6 weeks and 3 months

  3. Change in Serum creatinine

    Time frame: Weekly x 6 weeks, 1 longitudinal measurement at 3 months

    longitudinal change in Serum creatinine (mg/dl) over 6 weeks and 3 months

  4. Change in 1,25 dihydroxyvitamin D

    Time frame: Weekly x 6 weeks, 1 longitudinal measurement at 3 months

    longitudinal change in 1,25 dihydroxyvitamin D (pg/ml) over 6 weeks and 3 months

  5. Change in C-reactive protein

    Time frame: Weekly x 6 weeks, 1 longitudinal measurement at 3 months

    longitudinal change in C-reactive protein (mg/L) over 6 weeks and 3 months

  6. Change in Ferritin Measurement

    Time frame: Weekly x 6 weeks, 1 longitudinal measurement at 3 months

    longitudinal change in serum ferritin (ng/ml) over 6 weeks and 3 months

  7. Change in Iron Measurement

    Time frame: Weekly x 6 weeks, 1 longitudinal measurement at 3 months

    longitudinal change in Serum iron (ug/dl) over 6 weeks and 3 months

  8. Change in Transferrin Saturation

    Time frame: Weekly x 6 weeks, 1 longitudinal measurement at 3 months

    longitudinal change in Transferrin Saturation (%) over 6 weeks and 3 months

  9. Change in Hemoglobin Measurement

    Time frame: Weekly x 6 weeks, 1 longitudinal measurement at 3 months

    longitudinal change in Serum hemoglobin (g/dl) over 6 weeks and 3 months

Sponsors and collaborators

Lead sponsor

Northwestern University

Other

Collaborators

  • National Kidney Foundation, United States

Registry information

Official study title

Iron Deficiency and Fibroblast Growth Factor 23 Regulation in Chronic Kidney Disease and Heart Failure

Acronym: INDIGO

Important dates

Study start
2015
Primary completion
2018
Study completion
2018
First posted
Apr 10, 2017
Registry last updated
Mar 20, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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