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Clinical Trial to Assess the Influence of Gestational Stage and Maternal Age on Arterial Stiffness of the Mother

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ClinicalTrials.gov Identifier: NCT00180219
Recruitment Status : Withdrawn (recruitment failure)
First Posted : September 16, 2005
Last Update Posted : August 25, 2016
Sponsor:
Information provided by:
Technische Universität Dresden

Brief Summary:
This is a single-centre, open, parallel-group study with three age groups; no study medication or intervention will be provided. This is a longitudinal follow-up of physiological parameters.

Condition or disease
Pregnancy Trimester, First Pregnancy Trimester, Second Pregnancy Trimester, Third

Detailed Description:
The subjects will be investigated as outpatients. For each subject, 4 individual dates with a duration of approximately 30 minutes each are scheduled - at the end of the first trimenon, at the end of the second trimenon, 4 weeks prior to the calculated date of birth, and 6 weeks after the effective date of birth.

Study Type : Observational
Actual Enrollment : 0 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: An Open Clinical Trial to Assess the Influence of Gestational Stage and Maternal Age on Arterial Stiffness of the Mother (Hormonal and Age Related Changes of the Aortal Elasticity)
Study Start Date : January 2006
Actual Study Completion Date : June 2006

Group/Cohort
1
20 to 22 years
2
30 to 32 years
3
40 to 42 years




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Ages Eligible for Study:   20 Years to 42 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population
three age groups
Criteria

Inclusion Criteria:

  • Pregnant women without major concomitant disease
  • Willing and able to provide informed consent
  • Age (three age groups):

    • 20 to 22 years
    • 30 to 32 years
    • 40 to 42 years

Exclusion Criteria:

  • Non pregnant women
  • Men
  • No informed consent
  • Age not included in inclusion criteria
  • Major concomitant disease

Information from the National Library of Medicine

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): NCT00180219


Locations
Germany
Medizinische Fakultät der Technischen Universität Dresden
Dresden, Germany, 01307
Sponsors and Collaborators
Technische Universität Dresden
Investigators
Principal Investigator: Joachim Siegert, MD, DPharm, Phd Technische Universität Dresden

ClinicalTrials.gov Identifier: NCT00180219     History of Changes
Other Study ID Numbers: IKPD-S-01-04
First Posted: September 16, 2005    Key Record Dates
Last Update Posted: August 25, 2016
Last Verified: August 2016

Keywords provided by Technische Universität Dresden:
G08.520.769.550.408
G08.520.769.550.490
G08.520.769.550.520