NCT07193264

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

63
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for not_applicable

Timeline
25mo left

Started Oct 2025

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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

Study Progress22%
Oct 2025Jun 2028

First Submitted

Initial submission to the registry

September 18, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

September 25, 2025

Completed
6 days until next milestone

Study Start

First participant enrolled

October 1, 2025

Completed
2.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2027

Expected
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2028

Last Updated

September 29, 2025

Status Verified

September 1, 2025

Enrollment Period

2.2 years

First QC Date

September 18, 2025

Last Update Submit

September 24, 2025

Conditions

Keywords

Caffeine consumptioncaffeineHematopoietic Stem CellsHematopoietic Stem and Progenitor CellsEffect of caffeine on blood systemEffect of caffeine on hematopoietic system

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

EXPERIMENTAL

200mg Caffeine

Other: Caffeine (200 mg)

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.

Caffeine intervention

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Study Sites (1)

ETH GLC

Zurich, Canton of Zurich, 8006, Switzerland

Location

MeSH Terms

Interventions

Caffeine

Intervention Hierarchy (Ancestors)

XanthinesAlkaloidsHeterocyclic CompoundsPurinonesPurinesHeterocyclic Compounds, 2-RingHeterocyclic Compounds, Fused-Ring

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
SINGLE GROUP
Model Details: 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.
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

Locations