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NCT03526666 · ClinicalTrials.gov registry record
Ascorbic Acid Levels in MDS, AML, and CMML Patients
A clinical trial of Acute Myeloid Leukemia and Myelodysplastic Syndromes, sponsored by Van Andel Research Institute.
- Completed
- Registry status
- 50
- Enrollment target
- 2
- Study locations
NCT03526666: Completed study of Acute Myeloid Leukemia and Myelodysplastic Syndromes, sponsored by Van Andel Research Institute.
NCT03526666 is a study of Acute Myeloid Leukemia and Myelodysplastic Syndromes that has completed, run by Van Andel Research Institute. The registered enrollment target is 50 participants, below the 116-participant average among 306 other Acute Myeloid Leukemia trials with a reported enrollment target (57% lower). The trial reports 2 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03526666, a study of Acute Myeloid Leukemia and Myelodysplastic Syndromes, has completed, sponsored by Van Andel Research Institute.
- COMPLETED
- Registry status
- 50 participants
- Enrollment target
- 2
- Study locations
Study Summary
This study is a non-interventional, specimen collection translational study to evaluate vitamin C levels in the peripheral blood of Acute Myeloid Leukemia (AML), Myelodysplastic Syndrome (MDS), or Chronic Myelomonocytic Leukemia (CMML) patients.
Primary Outcome
The level of ascorbic acid
Conditions Studied
Interventions
- OTHER Peripheral blood collection
Study Locations (2)
Michigan
- Cancer and Hematology Centers of Western Michigan - Grand Rapids
- Metro Health - University of Michigan Health - Wyoming
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2017-11-01 |
| Est. Completion | 2018-10-31 |
What the finished NCT03526666 record still lists
NCT03526666 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 116-participant average among 306 other Acute Myeloid Leukemia trials with a reported enrollment target (57% lower).
The record links to 6 conditions, with Acute Myeloid Leukemia appearing as the primary indexed condition, and to 1 intervention - of which Peripheral blood collection is the first listed.
NCT03526666 reports a single indexed study location in Michigan.
Frequently Asked Questions
What is clinical trial NCT03526666 about?
NCT03526666 is a clinical study titled "Ascorbic Acid Levels in MDS, AML, and CMML Patients". This study is a non-interventional, specimen collection translational study to evaluate vitamin C levels in the peripheral blood of Acute Myeloid Leukemia (AML), Myelodysplastic Syndrome (MDS), or Chronic Myelomonocytic Leukemia (CMML) patients.
What is the current status of trial NCT03526666?
This trial is currently completed. The enrollment target is 50 participants. The study started on 2017-11-01. Estimated completion is 2018-10-31.
What conditions does trial NCT03526666 study?
This clinical trial studies the following conditions: Acute Myeloid Leukemia, Myelodysplastic Syndromes, Chronic Myelomonocytic Leukemia, AML, MDS.
What interventions are being tested in trial NCT03526666?
The interventions under investigation include: Peripheral blood collection (OTHER).
Who is sponsoring clinical trial NCT03526666?
This trial is sponsored by Van Andel Research Institute, which has 3 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03526666 being conducted?
This trial has 2 study locations across Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Where NCT03526666's enrollment target sits among peer trials
50 143rd of 306 higher than 154 of 306 other Acute Myeloid Leukemia trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Acute Myeloid Leukemia trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
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