Combined Novel 3D Cell Culture and Biospectroscopy: Osteoporosis

  • Research type

    Research Study

  • Full title

    Combined Novel 3D Cell Culture and Biospectroscopy; personalising Osteoporosis therapeutics

  • IRAS ID

    220163

  • Contact name

    JG Kerns

  • Contact email

    j.kerns@lancaster.ac.uk

  • Sponsor organisation

    Lancaster University

  • Duration of Study in the UK

    1 years, 5 months, 31 days

  • Research summary

    Osteoporosis is a debilitating progressive disease associated with ageing, particularly postmenopausal women. It is a serious international healthcare burden, which will increase as the ageing population grows. It is caused by a reduction in bone mineral density, which leads to fragile bones with an increased risk of fracture upon a low impact fall. There are now many different treatments available, the first line is a bisphosphonate. However, many may try different types or need to swap after several years. This is partly due to the x-ray radiation risk associated with the diagnostic tool, which is only recommended to be used every 3 years so the impact of the treatment cannot be easily assessed for improved bone quality. Secondly, bisphosphonates have been strongly linked to atypical fractures (an unusual mid-thigh fracture), which does not heal well and often leads to morbidity. The overall costs associated with diagnosis, treatment, management and fracture repair are a huge health-economic burden and severely reduces quality of life for the individual.
    The aim of this project is to provide a stratified medicine approach to osteoporosis treatment, which establishes the optimal treatment for the individual, off-line in a laboratory. This will leads to a reduction in a the amount of time taken to determine appropriate treatment, improved quality of life, and a reduction in atypical fractures associated with long-term treatment.

  • REC name

    London - Surrey Borders Research Ethics Committee

  • REC reference

    17/LO/0605

  • Date of REC Opinion

    27 Apr 2017

  • REC opinion

    Further Information Favourable Opinion