Houston, TXNCT05304442Now EnrollingIRB Ready

Anemia, Iron Deficiency Clinical Trial in Houston, TX

Access cutting-edge anemia, iron deficiency treatment through this clinical trial at a research site in Houston. Study-provided care at no cost to qualified participants.

Sponsored by Baylor College of Medicine

Quick Self-Assessment

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Expert Care in Houston

Access anemia, iron deficiency specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related anemia, iron deficiency treatment provided free

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Check if you qualify for this anemia, iron deficiency clinical trial in Houston, TX

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Houston

    Convenient for TX residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Houston site if eligible
  4. 4Begin participation

About This Anemia, Iron Deficiency Study in Houston

The primary aim of this randomized trial is to assess the efficacy of IV Ferric Derisomaltose vs Oral Iron in the management of women with severe Iron Deficiency Anemia due to Uterine Bleeding in the emergency department.

Sponsor: Baylor College of Medicine

Who Can Participate

Inclusion Criteria

Sub-acute or chronic uterine blood loss;
Moderate to Severe Anemia, defined as Hgb less than or equal to 9.0 g/dl;
Iron deficiency: Serum ferritin less than or equal to 30 ng/mL;
Eligible for discharge from the ED following treatment;
Patient able to return for planned follow-up visits at 3 and 6 weeks;
Patient able to be reached by telephone;
Willing and able to provide consent for participation.

Exclusion Criteria

Patient requiring hospitalization for any reason;
Pregnant or nursing;
Incarcerated/Prisoner;
Weight \< 50 kg;
History of hypersensitivity reactions, as specified, known hypersensitivity to any formulation of parenteral iron;
History of any anaphylactic allergy;
Recent receipt of IV iron, erythropoiesis-stimulating agents;
Erythropoiesis-stimulating agent use within 8 weeks prior to ED visit;
Parenteral iron within 4 weeks prior to ED visit;
Scheduled/planned use of parenteral iron or ESA during study period;
Receipt of blood transfusion at index visit;
Planned elective major surgery during study period;
Other current or recent hematologic therapy, as specified;
Current or planned use of antithrombotic therapy (antiplatelet agents or anticoagulants) within study period (Non-aspirin NSAIDs are NOT a contraindication);
Known bleeding disorder platelets \< 100,000';
Other significant underlying comorbidity, as specified:
Active rheumatologic disease, or rheumatologist disease requiring treatment, such as rheumatoid arthritis, systemic lupus erythematosus, or mixed connective tissue disease;
Acute heart failure or NYHA II-IV chronic heart failure;
Inflammatory bowel disease;
Cirrhosis or Decompensated liver disease;
Chronic kidney disease, stage III or greater (eGFR \< 60);
Current Systemic Infection (e.g. pneumonia, pelvic inflammatory disease, pyelonephritis). \*Cystitis or cervicitis is NOT an exclusion
Any other medical or surgical condition that in the opinion of the treating physician may result in patient being unsuitable for trial participation

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Houston?

Yes, this clinical trial (NCT05304442) has an active research site in Houston, TX that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Anemia, Iron Deficiency Treatment Options in Houston, TX

If you're searching for anemia, iron deficiency treatment options in Houston, TX, this clinical trial (NCT05304442) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Houston research site is actively enrolling participants for this clinical trial. You'll receive care from experienced anemia, iron deficiency specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all anemia, iron deficiency clinical trials near you to find additional studies recruiting in your area.

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