Actively Recruiting

Phase Not Applicable
Age: 20Years - 89Years
FEMALE
Healthy Volunteers
NCT06683222

Mediating Role of Myokines in the Dialogue Between Muscle and Bone Tissue in a Population of Healthy Women Aged 20-89 Years

Led by Centre Hospitalier Universitaire de Nīmes · Updated on 2024-11-29

280

Participants Needed

2

Research Sites

255 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The main hypothesis is that muscle acts on bone tissue via the secretion of myokines (myostatin, follistatin, irisin). This is based on previous results showing that muscle mass in different patient populations with very different body mass indexes (anorexic or obese patients) is significantly and independently associated with bone mineral density.

CONDITIONS

Official Title

Mediating Role of Myokines in the Dialogue Between Muscle and Bone Tissue in a Population of Healthy Women Aged 20-89 Years

Who Can Participate

Age: 20Years - 89Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Self-reported Caucasian ethnicity from Europe, Middle East, or North Africa
  • Affiliated with or benefiting from a social security scheme
  • Signed free and informed consent before any study examinations
Not Eligible

You will not qualify if you...

  • Fragility fracture from spontaneous or low-impact trauma
  • Early menopause before age 40, hysterectomy before 40, primary amenorrhea before 15, or current amenorrhea over 3 months without contraception if under 40
  • Prolonged corticosteroid therapy over 3 months or cumulative dose over 1 g
  • Immobilization lasting more than 3 months within the past 12 months
  • Hip fracture in a first-degree relative
  • Bone, muscle, or fat tissue diseases such as inflammatory bowel disease, untreated celiac disease, renal failure on dialysis, hypercalciuria, osteomalacia, rickets, osteogenesis imperfecta, Paget's disease, osteopetrosis, chronic inflammatory rheumatism, blood disorders, cancer, liver failure or chronic hepatitis, endocrine disorders including diabetes and untreated acromegaly, anorexia nervosa, hyperparathyroidism
  • History of digestive surgery except appendectomy
  • History of organ transplantation
  • Chronic infectious diseases like HIV
  • Weight loss of more than 10 kg in the last 6 months
  • Paresis, significant lameness, or prolonged immobilization over one month in the last year
  • Treatments affecting bone mass or body composition such as bisphosphonates, teriparatide, denosumab, selective estrogen receptor modulators, anabolic steroids, strontium ranelate, carbamazepine, phenobarbital, immunosuppressants, or anti-epileptics
  • Major deformities or previous surgeries affecting wrist, hip, or vertebrae in measurement areas
  • Recent injections of radiological contrast, barium enemas, or nuclear medicine exams within 10 days
  • Intensive sports activity over 10 hours per week
  • Extreme body mass index below 18 or above 35 kg/m2
  • Loss of autonomy or neurodegenerative disorders affecting consent ability
  • Pregnant, parturient, or breastfeeding women
  • Participation in an interventional drug or device study within 3 months prior to inclusion

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

C.H.R.U. Lapeyronie

Montpellier, France, 34295

Actively Recruiting

2

Chu Nimes

Nîmes, France, 30029

Actively Recruiting

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Research Team

V

Vincent BOUDOUSQ, Dr

CONTACT

A

Anissa MEGZARI

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

1

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