Restoring Iron Deficiency in POTS

Purpose

People with postural orthostatic tachycardia syndrome (POTS) often have low red blood cell volumes and low ferritin in their blood (a marker of iron storage in the body). The purpose of this pilot study is to investigate whether giving iron to people with POTS who have low ferritin levels will increase the red blood cell volume and improve POTS symptoms.

Condition

  • POTS - Postural Orthostatic Tachycardia Syndrome

Eligibility

Eligible Ages
Between 18 Years and 45 Years
Eligible Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Age 18-45 years old. - Diagnosis of POTS, defined by a sustained heart rate increase of at least 30 bpm within 10 min of standing or head-up tilt (or absolute upright heart rate >120 bpm), in the absence of orthostatic hypotension, and with at least 3 months of symptoms of orthostatic intolerance. - Absence of other diseases or medications that can explain orthostatic tachycardia or symptoms. - Serum ferritin <50 ng/ml. - Patients on fludrocortisone will be allowed to participate as long as they have been on the same dose for at least one month before enrollment and continue on the same dose throughout the study.

Exclusion Criteria

  • Unable or unwilling to provide consent. - Pregnancy. - Being chair- or bed-ridden. - Unable to hold POTS medications during study procedures (i.e., autonomic testing). - History of active bleeding (other than menstruation). - History of hypersensitivity to any iron preparation of recent (within 6 months) treatment with any IV iron preparation.

Study Design

Phase
Phase 2
Study Type
Interventional
Allocation
N/A
Intervention Model
Single Group Assignment
Primary Purpose
Treatment
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Intravenous Iron Infusion
The Intravenous iron infusion will be administered according to standard clinical care.
  • Drug: Intravenous iron
    The Intravenous iron infusion will be administered according to standard clinical care. The provider will choose the dosage and formulation of IV iron.

Recruiting Locations

Autonomic Dysfunction Center/ Vanderbilt University Medical Center
Nashville 4644585, Tennessee 4662168 37232

More Details

Status
Recruiting
Sponsor
Vanderbilt University Medical Center

Study Contact

Megan Orillion, BSN, RN
615-875-9405
autonomics@vumc.org

Detailed Description

This pilot study involves undergoing a physical exam and medical history, answering some questionnaires, and visiting the Vanderbilt Autonomic Dysfunction Center before and 2 months after the iron treatment for bloodwork, blood volume measurements, autonomic function tests, and wearing an activity monitor.