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Impact of Chronic and Acute Caffeine Intake on the Hematopoietic System

CaffeineHSC - Effect of Chronic Caffeine Consumption and Acute Caffeine Administration on the Hematopoietic System

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07193264
Acronym
CaffeineHSC
Enrollment
100
Registered
2025-09-25
Start date
2025-10-31
Completion date
2028-06-30
Last updated
2025-09-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy Adults; Hematopoietic System; Caffeine

Keywords

Caffeine consumption, caffeine, Hematopoietic Stem Cells, Hematopoietic Stem and Progenitor Cells, Effect of caffeine on blood system, Effect of caffeine on hematopoietic system

Brief summary

This study investigates how caffeine intake affects blood stem and progenitor cells in healthy adults. The trial will compare people who regularly consume caffeine with those who consume very little or none. All participants will receive a single 200 mg caffeine tablet (similar to one cup of coffee) under fasting conditions. Blood samples will be collected before and three hours after caffeine intake. The study will assess whether caffeine influences the mobilization of blood stem and progenitor cells from the bone marrow into the bloodstream. It will also examine the effects of caffeine on the function, gene activity, and metabolism of blood cells.

Interventions

Participants receive a single oral dose of 200 mg caffeine under fasting conditions. Blood samples are collected before and three hours after intake to evaluate effects on hematopoietic stem and progenitor cells, including mobilization, function, gene expression, and metabolism.

Sponsors

ETH Zurich
CollaboratorOTHER
Laboratory of Stem Cell Biology and Ageing, ETH Zurich, Prof. Nina Cabezas-Wallscheid
CollaboratorUNKNOWN
Prof. Dr. Nina Cabezas-Wallscheid, ETH Zurich
CollaboratorUNKNOWN
Jasmin Rettkowski
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Intervention model description

This is a single-group, open-label study in which all participants receive a single oral dose of 200 mg caffeine under fasting conditions. Blood samples are collected before and three hours after caffeine intake to assess mobilization, function, gene expression, and metabolic profile of hematopoietic stem and progenitor cells.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Able to give consent. * Healthy adults aged ≥ 18 years. * Regular caffeine consumers (≥1 coffee cup/day or ≥1 energy drink/day) or non-consumers (≤1 cup/month and ≤1 energy drink/month) for at least 6 months. * Willingness to comply with fasting requirements and study procedures.

Exclusion criteria

* Chronic illnesses or medication use affecting metabolism, including metabolic disorders (e.g., diabetes, thyroid dysfunction, metabolic syndrome). * Personal history of cancer. * Personal history of hematological disorders. * History of radiation therapy. * Known caffeine hypersensitivity or intolerance. * Known immunosuppression.

Design outcomes

Primary

MeasureTime frameDescription
Mobilization of hematopoietic stem and progenitor cellsFrom baseline to three hours after caffeine intakeThe change in the numbers of mobilized HSPCs (defined as CD34+ cells) \[cells/ml\] in blood (measured by flow cytometry) from baseline to three hours after intake of a single oral dose of 200mg caffeine in habitual caffeine consumers versus non-caffeine consumers.

Secondary

MeasureTime frameDescription
Functional alterations in CD34+ peripheral blood cellsFrom baseline to three hours after caffeine intakeFunctional alterations in CD34+ PB cells: self-renewal \[number of colonies\] assessed via colony-forming unit assay.
Transcriptional changes in CD34+ cellsFrom baseline to three hours after caffeine intakeTranscriptional changes in CD34+ cells \[log2 fold change in gene expression and DEG count\] assessed via single-cell RNA sequencing.
Relative metabolite abundanceFrom baseline to three hours after caffeine intakeRelative metabolite abundance \[arbitrary units based on peak area or height in LC-MS\] in plasma and intracellularly in isolated CD34+ cells.
Change in the numbers of peripheral blood cellsFrom baseline to three hours after caffeine intakeThe change in the numbers of PB cells \[cells/ml\], including B cells, T cells, myeloid cells in blood, and relative, and measured by flow cytometry

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026