Recruiting NA Acute Leukemia

New treatment option for Acute Leukemia

Official title Biomarkers in Patients With Anemia-Induced Thrombocytopenic Bleeding

ClinicalTrials.gov ID: NCT06947044

What this study is testing

What it's testing
This pilot study aims to gather preliminary evidence on how different hemoglobin levels impact blood biomarkers related to bleeding. The feasibility of conducting a future larger clinical trial will also be assessed.

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 18 and older

You may be able to join if

  • ≥18 years old.
  • Inpatient
  • Diagnosis of acute myeloid leukemia or acute lymphocytic leukemia.
  • Less than 5 days have elapsed since the start of induction chemotherapy treatment.
  • Hemoglobin at enrolment is under 130 g/L.

You likely can't join if

  • Failure to provide informed consent.
  • Unwilling to receive blood transfusions.
  • Life expectancy \<72 hours.
  • Undergoing palliative chemotherapy.
  • Requires specialized blood products (e.g., antigen-matched, irradiation, etc.).
  • Diagnosis of acute promyelocytic leukemia.
See the full eligibility criteria
Who can join
  • ≥18 years old.
  • Inpatient
  • Diagnosis of acute myeloid leukemia or acute lymphocytic leukemia.
  • Less than 5 days have elapsed since the start of induction chemotherapy treatment.
  • Hemoglobin at enrolment is under 130 g/L.
What rules you out
  • Failure to provide informed consent.
  • Unwilling to receive blood transfusions.
  • Life expectancy \<72 hours.
  • Undergoing palliative chemotherapy.
  • Requires specialized blood products (e.g., antigen-matched, irradiation, etc.).
  • Diagnosis of acute promyelocytic leukemia.
  • Diagnosis of hyperleukocytosis (a white blood cell count exceeding 100 × 10\^9/L).
  • Diagnosed with coagulopathies or ongoing treatment with therapeutic anticoagulants, aspirin or nonsteroidal anti-inflammatory drugs (history of inherited or acquired coagulation disorder, known hemolytic disease, INR \>...
  • Evidence of iron overload (ferritin \>800 ng/mL, transferrin saturation \>80%) .

The study team makes the final eligibility decision.

Where it's taking place

  • Hamilton, Ontario, Canada

Compensation & support

Compensation mentioned.

ClinicalTrials.gov doesn't provide a reliable structured field for payment or travel support - confirm details with the study team.

Questions & answers

Do participants get paid in this trial?

This study's listing includes signals that participants may be compensated or receive a stipend. Amounts vary and are set by the study team - confirm the details with them.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Hamilton, Ontario, Canada. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.