Impact of Chronic and Acute Caffeine Intake on the Hematopoietic System
CaffeineHSC
CaffeineHSC - Effect of Chronic Caffeine Consumption and Acute Caffeine Administration on the Hematopoietic System
1 other identifier
interventional
100
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Oct 2025
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 18, 2025
CompletedFirst Posted
Study publicly available on registry
September 25, 2025
CompletedStudy Start
First participant enrolled
October 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
June 1, 2028
September 29, 2025
September 1, 2025
2.2 years
September 18, 2025
September 24, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Mobilization of hematopoietic stem and progenitor cells
The 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.
From baseline to three hours after caffeine intake
Mobilization of hematopoietic stem and progenitor cells
The change in the relative abundance of HSPCs \[% HSPCs of total PBMCs\] 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.
From baseline to three hours after caffeine intake
Secondary Outcomes (6)
Functional alterations in CD34+ peripheral blood cells
From baseline to three hours after caffeine intake
Functional alterations in CD34+ peripheral blood cells
From baseline to three hours after caffeine intake
Transcriptional changes in CD34+ cells
From baseline to three hours after caffeine intake
Relative metabolite abundance
From baseline to three hours after caffeine intake
Change in the numbers of peripheral blood cells
From baseline to three hours after caffeine intake
- +1 more secondary outcomes
Study Arms (1)
Caffeine intervention
EXPERIMENTAL200mg Caffeine
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.
Eligibility Criteria
You may qualify if:
- 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.
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Jasmin Rettkowskilead
- ETH Zurichcollaborator
- Laboratory of Stem Cell Biology and Ageing, ETH Zurich, Prof. Nina Cabezas-Wallscheidcollaborator
- Prof. Dr. Nina Cabezas-Wallscheid, ETH Zurichcollaborator
Study Sites (1)
ETH GLC
Zurich, Canton of Zurich, 8006, Switzerland
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Dr. Jasmin Rettkowski, Principal Investigator, Department of Health Sciences and Technology, ETH Zurich
Study Record Dates
First Submitted
September 18, 2025
First Posted
September 25, 2025
Study Start
October 1, 2025
Primary Completion (Estimated)
December 1, 2027
Study Completion (Estimated)
June 1, 2028
Last Updated
September 29, 2025
Record last verified: 2025-09
Data Sharing
- IPD Sharing
- Will share