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Bone Microarchitecture in Young Cystic Fibrosis Patients

Evaluation of the Bone Microarchitecture in a Young Cystic Fibrosis Patients Using High-Resolution Peripheral Quantitative Computed Tomography

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01788267
Enrollment
38
Registered
2013-02-11
Start date
2013-01-31
Completion date
2015-05-31
Last updated
2019-05-28

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

Conditions

Cystic Fibrosis

Keywords

Cystic Fibrosis, High-Resolution peripheral Quantitative Computed Tomography, Bone Mass Density

Brief summary

Patients with cystic fibrosis are at risk of developing low bone mineral density (BMD) potentially leading to pathological fractures at adult age. Recent data from our center and others have suggested that low BMD could be observed very early in life. However, quantitative bone abnormalities found out by Dual X-ray absorptiometry (DXA) need to be confronted to qualitative evaluation of bone microarchitecture (surrogate of bone strength). High-Resolution peripheral quantitative computed tomography (HR-pQCT) is a recent technology with very high spatial resolution. Images obtained with this technic are considered as virtual bone biopsies. It enables an accurate bones' cortical and trabecular surfaces exploration in a three-dimensional manner, and therefore provides informations on bone microarchitecture as well as bone density. The aim of this study is to evaluate bone microarchitecture of paediatric patients matched to sex-age-pubertal status-healthy volunteers. In the meantime, biological markers will be collected and DXA (Dual-energy x-ray absorptiometry) will be performed in order to explore potential correlations HR-pQCT parameters.

Interventions

OTHERscan examination HR-pQCT

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
10 Years to 18 Years
Healthy volunteers
Yes

Inclusion criteria

* Cystic Fibrosis patient of both sex * Pubertal patient * Age ≥10 years and ≤18 years on the date of informed consent * FEV1(forced expiratory volume at one second ) ≥ 60% of predicted normal for age, gender and height * Patient on a clinical stable period

Exclusion criteria

* Unable to maintain arm and/or leg immobile for 3 minutes * History of solid organ transplantation * Participation in the same time to a clinical trial * Acute pulmonary exacerbation at the time of evaluation

Design outcomes

Primary

MeasureTime frame
Total Tibial Bone Mass Density measured by High-Resolution peripheral Quantitative Computed Tomographyat the inclusion visit J0

Secondary

MeasureTime frame
total radial bone mass densityat the inclusion visit J0
Trabecular bone micro-architecture at tibia and radial sitesat the inclusion visit J0
Biological markers : 1) bone markers : parathyroid hormone (PTH), Calcifediol (25(OH)D3), osteocalcin, Endocrinal markers : IGF-1 (insulin like growth factor ), IGFBP-3, leptin, adiponectin, visfatin, resistinat the inclusion visit J0

Countries

France

Outcome results

None listed

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