Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 1:12 AM
Ignite Modification Date:
2025-12-25 @ 1:12 AM
NCT ID:
NCT01144793
Eligibility Criteria:
Inclusion Criteria:- Age \>= 18
* Pre-admission (ATU, ITA) or inpatient status
* absolute neutrophil count (ANC) \<= 1500/mm\^3
* Patients with acute myeloid or lymphoid leukemia who:
* are admitted with newly diagnosed disease and have not yet received induction chemotherapy
* are admitted with neutropenic fever after receiving post-remission chemotherapy or are admitted for post-remission chemotherapy
* Patients with chronic myeloid leukemia or a chronic lymphoid leukemia/disorder who have received chemotherapy or other disease-specific treatment in the last 30 days where the ANC of \<=1500/mm3 is considered by the treating physician to be at least possibly treatment-related
* An intravenous line or catheter (Hickman, port, portacath, or peripherally inserted central venous catheter \[PICC\] line) must be in place at the time of protocol participation/study start, but will not be inserted solely for the purposes of the study.
* Whenever possible, patients will be consented and blood monitoring will be initiated before the first dose of antibiotic, but if not possible, at no time will standard of care measures will be delayed or interrupted for the purposes of study enrollment.
* Patients must be able to understand the nature of the study and give written informed consent.
There are no exclusion criteria. Anyone who does not meet inclusion criteria will be excluded.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT01144793
Study Brief:
Protocol Section:
NCT01144793