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Arteos II Study: Relationship Between Osteoporosis and Arterial Rigidity Within Fractured Patients Cohort (ARTEOS2)

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ClinicalTrials.gov Identifier: NCT01587456
Recruitment Status : Unknown
Verified June 2016 by Central Hospital, Nancy, France.
Recruitment status was:  Recruiting
First Posted : April 30, 2012
Last Update Posted : June 16, 2016
Sponsor:
Information provided by (Responsible Party):
Central Hospital, Nancy, France

Brief Summary:
The investigators planned to study relationship between osteoporosis and arterial rigidity within fractured patients cohort.

Condition or disease
Osteoporosis

Study Type : Observational
Estimated Enrollment : 300 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Relationship Between Osteoporosis and Arterial Rigidity Within Fractured Patients Cohort.
Study Start Date : April 2012
Estimated Primary Completion Date : April 2017
Estimated Study Completion Date : April 2017

Resource links provided by the National Library of Medicine





Biospecimen Retention:   Samples With DNA
Serum, Plasma and DNA


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Ages Eligible for Study:   60 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Women and men > 60 years of age with medical history of low energy fracture andradiologic osteoporosis with DXA Tscore at -2,5 DS.
Criteria

Inclusion Criteria:

  • women and men > 60 years of age
  • medical history of low energy fracture
  • DXA Tscore -2,5 DS
  • FREE AND INFORMED CONSENT SIGNED

Exclusion Criteria:

  • women and men < 60 years of age
  • Corticoids treatment
  • Breast cancer or prostat cancer medical history
  • High energy fracture (traumatic fracture)
  • No social security affiliation
  • Incapacity to informed consent signed.

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To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01587456


Contacts
Contact: Georges WERYHA, MD, PHD 33 3 83 15 35 05 g.weryha@chu-nancy.fr
Contact: Anna KEARNEY SCHWARTZ, MD +33 3 83 15 33 22 a.kearney-schwartz@chu-nancy.fr

Locations
France
CHU de Brabois Endocrinology Recruiting
Vandoeuvre, France, 54500
Contact: Georges WERYHA, Professor    33 3 83 15 35 05    g.weryha@chu-nancy.fr   
Contact: Anna KEARNEY-SCHWARTZ, Doctor    33 3 83 15 33 22    a.kearney-schwartz@chu-nancy.fr   
Principal Investigator: Georges WERYHA, Professor         
Sub-Investigator: Anna KEARNEY SCHWARTZ, Doctor         
Sub-Investigator: Anna ANGELOUSI, Doctor         
Sub-Investigator: Athanase BENETOS, Professor         
Sub-Investigator: Shiva KHORSAND, Doctor         
Sub-Investigator: Lelia GROZA, Doctor         
Sub-Investigator: Eva FEIGERLOVA, Doctor         
Sub-Investigator: Paolo SALVI, Professor         
Sponsors and Collaborators
Central Hospital, Nancy, France
Investigators
Principal Investigator: Georges WERYHA, Professor CHU de Brabois Endocrinology

Responsible Party: Central Hospital, Nancy, France
ClinicalTrials.gov Identifier: NCT01587456     History of Changes
Other Study ID Numbers: 2011-A00453-38
First Posted: April 30, 2012    Key Record Dates
Last Update Posted: June 16, 2016
Last Verified: June 2016
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided

Keywords provided by Central Hospital, Nancy, France:
Osteoporosis

Additional relevant MeSH terms:
Osteoporosis
Bone Diseases, Metabolic
Bone Diseases
Musculoskeletal Diseases
Metabolic Diseases