Clinical trial · Observational
Pre and Post Treatment Metabolomic Analysis of Leukemia: A Translational Clinical Trial of the Brown Cancer Center
PRE AND POST TREATMENT METABOLOMIC ANALYSIS OF LEUKEMIA: A Translational Clinical Trial of the Brown Cancer Center
NCT02193100CI-TRIAL-00030974withdrawnClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
To characterize the metabolism of glucose by the leukemic cells in patients with leukemia before and after initial chemotherapy. To compare the metabolism of glucose by leukocytes in healthy volunteers and leukemic cells in leukemic patients.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Leukemia | Leukemia | ONTOLOGY_EXACT | 0.90 |
Interventions
Interventions (0)
Data not yet available
No intervention recorded.
Design
Arms and outcomes
Arms (2)
- label
- 13C-glucose
- description
- experimental (13C-glucose)
- label
- No glucose
- description
- control (no glucose)
Primary outcomes (1)
- measure
- Metabolic characteristics of leukemic cells from blood and urine samples using nuclear magnetic resonance spectroscopy (NMR)
- timeFrame
- Baseline up to 6 months post treatment
- description
- Blood and urine samples will be taken before and after chemotherapy treatment for up to 6 months post treatment and analyzed for metabolic substances using nuclear magnetic resonance (NMR) spectroscopy with intergraded hyphenated mass spectrometry.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria for Leukemia Subjects: * Each of the criteria in the following section must be met in order for a patient to be eligible for enrollment. * Only patients with clinically diagnosed or histologically diagnosed leukemia will be eligible to participate in this non-therapeutic study. * All patients must have measurable quantities of leukemic blasts on peripheral blood detected with a CBC. * No history of diabetes for the experimental group or the control group. * Patients with known hepatitis C or HIV (AIDS) are excluded. * Patients must be informed of the investigational nature of this study and sign and give written informed consent in accordance with institutional and federal guidelines. Inclusion Criteria forHealthy Subjects: * Subjects must have no known prior history of cancer or malignant blood disorders. -Where possible, follow up will be carried out to verify that no cancer has developed since the blood collection. This will be done by a phone call performed one month from sample to ask if new medical conditions have arisen. * Subjects must have WBC, RBC, and platelet counts within normal range on CBC. * Subjects with known hepatitis C or HIV (AIDS) are excluded. * No history of Diabetes * At least 30 years of age * Preferably be fasting for 12 hours (minimum 8 hours) prior to enrollment * Patients must be informed of the investigational nature of this study and sign and give written informed consent in accordance with institutional and federal guidelines. Exclusion Criteria: * None listed in protocol
References
Publications (0)
Data not yet available
No reference posted for this study.