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Microbiota Changes in Acute Myeloid Leukemia Patients Undergoing Intensive Chemotherapy

University of Minnesota (UMN) logo

University of Minnesota (UMN)

Status

Completed

Conditions

Acute Myeloid Leukemia

Treatments

Diagnostic Test: Stool Sample
Diagnostic Test: Sample Collection Blood

Study type

Observational

Funder types

Other

Identifiers

NCT03728699
HM2018-23 (Other Identifier)
2018NTLS107

Details and patient eligibility

About

This is a prospective, observational study to collect stool and blood from acute myeloid leukemia patients undergoing intensive chemotherapy.

Enrollment

54 patients

Sex

All

Ages

18 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Adults (ages 18 - 99 years) undergoing inpatient intensive chemotherapy for newly diagnosed, refractory, or relapsed AML. Patients may or may not have been exposed to any type of therapy before.
  • Any intensive chemotherapy regimen defined as a planned ~4 week inpatient stay. Chemotherapy may be delivered for any number of days and on any schedule. Patients may be discharged from the hospital sooner than 4 weeks if the treating physician choose so, but the expectation at the initiation of chemotherapy must be ~4 weeks of inpatient stay, as is typical.
  • Able to provide written voluntary consent before performance of any study related procedure.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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