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

This study has been withdrawn prior to enrollment.
(recruitment failure)
Sponsor:
ClinicalTrials.gov Identifier:
NCT00180219
First Posted: September 16, 2005
Last Update Posted: August 25, 2016
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Technische Universität Dresden
  Purpose
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 Phase
Pregnancy Trimester, First Pregnancy Trimester, Second Pregnancy Trimester, Third Phase 1

Study Type: Observational
Study Design: 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)

Further study details as provided by Technische Universität Dresden:

Enrollment: 0
Study Start Date: January 2006
Study Completion Date: June 2006
Groups/Cohorts
1
20 to 22 years
2
30 to 32 years
3
40 to 42 years

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.
  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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
  Contacts and Locations
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
  More Information

ClinicalTrials.gov Identifier: NCT00180219     History of Changes
Other Study ID Numbers: IKPD-S-01-04
First Submitted: September 14, 2005
First Posted: September 16, 2005
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