Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05750654

Effectiveness of Small Phlebotomy Tubes in Reducing Blood Transfusions in Adult Medical Intensive Care Unit and Intermediate Care Unit Patients With Anemia

Led by The University of Texas Health Science Center, Houston · Updated on 2025-09-10

688

Participants Needed

1

Research Sites

131 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this study is to evaluate the effectiveness of small phlebotomy tubes to reduce RBC transfusions in medical intensive care unit (ICU) and Intermediate care unit (IMU) patients with low hemoglobin compared with standard size tubes, to compare the intervention and the control groups in regards to: ICU length of stay (LOS), ICU mortality, hospital LOS, and hospital mortality and to assess the acceptability of small phlebotomy tubes in adult ICU and IMU patients.

CONDITIONS

Official Title

Effectiveness of Small Phlebotomy Tubes in Reducing Blood Transfusions in Adult Medical Intensive Care Unit and Intermediate Care Unit Patients With Anemia

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Admission to the medical ICU or IMU
  • Hemoglobin less than 10 g/dL
Not Eligible

You will not qualify if you...

  • Clinical bleeding requiring intervention such as increased hemoglobin monitoring, transfusion, procedure, or consultation
  • Hemolytic disorders such as sickle cell disease, hereditary spherocytosis, or autoimmune hemolytic anemia
  • Bone marrow disorders including aplastic anemia, leukemia, marrow infiltration disorder, or chemotherapy within the last 8 weeks
  • Jehovah's Witnesses
  • Patients receiving comfort care measures only
  • Refractory shock defined as mean arterial blood pressure below 65 mmHg despite maximal doses of 3 vasopressors
  • Severe acidosis with pH below 7 in more than one arterial blood gas in the past 24 hours (unless diabetic ketoacidosis)
  • Surgical admission diagnosis
  • Pregnancy
  • Current prisoner

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

The University of Texas Health Science Center at Houston

Houston, Texas, United States, 77030

Actively Recruiting

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Research Team

J

Javier Barreda Garcia, MD

CONTACT

I

Ibilola A Sanusi, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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