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Recruiting NCT05246813

Metabolic Profiling of Hematopoietic Stem Cells in Clonal Hematopoiesis (CHIP)

Observational Osteoporosis Osteoarthritis, Hip Hip Fractures Clonal Hematopoiesis of Indeterminate Potential

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Blood and bone marrow cell collection.
Who it may be relevant to
Registry conditions: Osteoporosis, Osteoarthritis, Hip, Hip Fractures, Clonal Hematopoiesis of Indeterminate Potential. Basic parameters: from 55 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Belgium
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Metabolic Profiling of Hematopoietic Stem Cells in Clonal Hematopoiesis (CHIP): a Prospective Observational Study

Overview

Bone marrow samples will be collected from patients undergoing hip arthroplasty surgery. Blood and bone marrow samples will be used for metabolic profiling and analysis of relevant CHIP mutations. Combined single-cell transcriptomics and mutation-specific single-cell genotyping (biotin-PCR using mutation-targeted primers followed by sequencing) will subsequently be performed. The gene expression profile of wildtype and mutant hematopoietic stem cells will be compared, performing both broad gene set enrichment analysis and targeted analysis of metabolic pathways.

Interventions

  • Other Blood and bone marrow cell collection
    Collection of blood and bone marrow

Primary outcome measures

  • Gene Set Enrichment Analysis (GSEA) Normalized Enrichment Score (NES) [Time frame: One day]

Eligibility criteria

Inclusion criteria

  • Age 65 years and older

Exclusion criteria

  • known haematological condition (myelodysplasia, leukemia, cancer)
  • inability to provide written informed consent

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-control

Study locations

Belgium · 1 center
  • Imelda Hospital — Bonheiden

Identifiers

NCT: NCT05246813 · 20211214

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗