- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02097888
Influence of Erythropoietin on Bone Marrow Microenvironment
March 24, 2014 updated by: PD Dr. med. Sandrine Meyer-Monard, Kantonsspital Baselland Bruderholz
Influence of Erythropoietin on Bone Marrow Microenvironment: A Pilot Study
This will be a prospective observational study.
The investigators will compare Erythropoietin (Epo) levels, erythropoiesis, and regulators of erythropoiesis, bone imaging and bone metabolism in healthy volunteers living at different altitudes.
Study Overview
Status
Unknown
Conditions
Study Type
Observational
Enrollment (Anticipated)
120
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Bruderholz, Switzerland, 4101
- Recruiting
- Kantonsspital Baselland / Bruderholz
-
Contact:
- Helga Schneider
- Phone Number: 0041 61 436 31 44
- Email: helga.schneider@ksbl.ch
-
Contact:
- Sandrine Meyer-Monard, PD Dr. med.
- Phone Number: 0041 61 436 2203
- Email: sandrine.meyer@ksbl.ch
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Principal Investigator:
- Sandrine Meyer-Monard, PD Dr. med.
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Residents living < 400m over sea level and >1500m over sea level
Description
Inclusion Criteria:
- healthy men and non-pregnant women, ages ≥18-40 years and ≥ 60 years living in the predefined area
- Exclusion Criteria:
- Known bone pathology including osteoporosis, known haematological disease, known renal disease, heart insufficiency, pulmonal disease
- pregnancy
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Difference of EPO level between control groups
Time Frame: up to 4 years
|
up to 4 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Sandrine Meyer-Monard, PD Dr. med., Kantonsspital Baselland / Bruderholz, Department of Medicine, Studienabteilung, CH-4101 Bruderholz
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
December 1, 2011
Primary Completion (Anticipated)
December 1, 2014
Study Completion (Anticipated)
December 1, 2014
Study Registration Dates
First Submitted
March 19, 2014
First Submitted That Met QC Criteria
March 24, 2014
First Posted (Estimate)
March 27, 2014
Study Record Updates
Last Update Posted (Estimate)
March 27, 2014
Last Update Submitted That Met QC Criteria
March 24, 2014
Last Verified
March 1, 2014
More Information
Terms related to this study
Other Study ID Numbers
- KSBLB: 252/11
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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