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OSTEOMICS: Identifying Regulators of Bone Homeostasis

OSTEOMICS: Identifying Regulators of Bone Homeostasis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05732870
Acronym
OSTEOMICS
Enrollment
2000
Registered
2023-02-17
Start date
2023-01-12
Completion date
2032-12-01
Last updated
2026-08-14

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

Conditions

Bone Diseases, Bone Fracture, Bone Marrow Disease, Osteoarthritis, Osteoporosis

Brief summary

Diseases of bone associated with ageing, including osteoporosis (OP) and osteoarthritis (OA), reduce bone mass, bone strength and joint integrity. Current non-surgical approaches are limited to pharmaceutical agents that are not disease modifying and have poor patient tolerability due to side effect profiles. Developing a fundamental understanding of cellular bone homeostasis, including how key cell types affect tissue health, and offering novel therapeutic targets for prevention of bone disease is therefore essential. This is the focus of OSTEOMICS. A number of factors have been linked to increased risk of bone disease, including genetic predisposition, diet, smoking, ageing, autoimmune disorders and endocrine disorders. In our study, we will recruit patients undergoing elective and non-elective orthopaedic surgery and obtain surgical bone waste for analysis. This will capture a cohort of patients with bone disorders like OP and OA, in addition to patients without overt clinical bone disease. We will study the relationship between the molecular biology of bone cells, bone structure, genetics (DNA) and environmental factors with the aim of identifying and validating novel therapeutic targets. We will leverage modern single cell technologies to understand the diversity of cell types found in bone. These technologies have now led to the characterisation of virtually every tissue in the body, however bone and bone-adjacent tissues are massively underrepresented due to the anatomical location and underlying technical challenges. Early protocols to demineralise bone and perform single cell profiling have now been developed. We will systematically scale up these efforts to observe how genetic variation at the population level leads to alterations in bone structure and quality. Over the next 10 years, we will generate data to comprehensively characterise bone across health and disease, use machine learning to drive analysis, and experimentally validate hypotheses - which will ultimately contribute to developing the next generation of therapeutic agents.

Interventions

PROCEDURERelevant orthopaedic surgery

Inclusion criteria is purposefully broad to examine a range of discarded bone waste. Therefore, a large number of surgical interventions are relevant.

Sponsors

Relation Therapeutics
Lead SponsorINDUSTRY
Harley Street Specialist Hospital
CollaboratorUNKNOWN
Fitzrovia Hospital
CollaboratorUNKNOWN
Royal Free Hospital NHS Foundation Trust
CollaboratorOTHER
Bedfordshire Hospitals NHS Foundation Trust
CollaboratorOTHER
Chelsea and Westminster NHS Foundation Trust
CollaboratorOTHER
Barts & The London NHS Trust
CollaboratorOTHER
Royal National Orthopaedic Hospital NHS Trust
CollaboratorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 110 Years

Inclusion criteria

1. Patients with osteoarthritis undergoing total joint arthroplasty, osteotomy or arthrodesis of any joint (including hip, knee, shoulder, wrist, elbow, ankle). 2. Patient with fractured neck of femurs undergoing hemiarthroplasty or total hip arthroplasty, or other internal fixation procedure. 3. Patients undergoing acute low-velocity or fragility fracture fixation surgery. 4. Patients aged between 18-110 years old with capacity to consent. Since deteriorating bone health including diseases like osteoporosis are primarily conditions of older age there is no practical upper age-limit. However, study involvement is limited by suitability for surgery which encompasses multiple factors considered on an individual case basis including age, frailty, comorbidities, baseline mobility, renal function and ability to consent (for instance due to dementia or delirium). We note that our inclusion criteria is purposefully broad as we aim to deduce trends across a wide range of conditions and backgrounds.

Exclusion criteria

1. Patients unable to provide informed consent. 2. Patients with suspected/established underlying malignancy. 3. Patients with suspected/established osteomyelitis. 4. Patients with suspected/established bloodborne disease 5. Patients who are currently a subject of a clinical trial involving an investigational medicinal product.

Design outcomes

Primary

MeasureTime frameDescription
Acquisition of bone wasteWithin 4 hours of resection.Discarded bone waste to be used for the study of RNA.

Secondary

MeasureTime frameDescription
Acquisition of 10ml of blood.Within 4 hours of resection.Discarded blood to be used for genetic sequencing, and/or other downstream omics/assays
Completion of participant questionnaireEDC entry within 1 week of surgery.Patient metadata to be used to understand cohort and identify confounding factors.

Countries

United Kingdom

Contacts

CONTACTJake Taylor-King, DPhil
jake@relationrx.com447387227904
CONTACTSusan O'Connor
susan.oconnor@blctrials.onmicrosoft.com07513017280
PRINCIPAL_INVESTIGATORRaghbir Khakha

Harley Street Specialist Hospital & Fitzrovia Hospital/QASMC

PRINCIPAL_INVESTIGATORAkash Patel

Royal Free London NHS Foundation Trust

PRINCIPAL_INVESTIGATORYegappan Kalairajah

Luton & Dunstable University Hospital, Bedfordshire Hospitals NHS Foundation Trust

PRINCIPAL_INVESTIGATORVictor Babu

Chelsea and Westminster NHS Foundation Trust

PRINCIPAL_INVESTIGATORJonathan Ward

Barts & The London NHS Trust

PRINCIPAL_INVESTIGATORRichard Keen

Royal National Orthopaedic Hospital NHS Trust

PRINCIPAL_INVESTIGATORInes Reichert

King's College Hospital NHS Trust

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 15, 2026