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Clinical Trial: Clinical Trial to Assess the Influence of Gestational Stage and Maternal Age on Arterial Stiffness of the Mother
This study is not yet open for patient recruitment.
Verified by Dresden University of Technology September 2005
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Purpose
Single-centre, open, parallel-group study with three age groups; no study medication or intervention. Longitudinal follow up of physiological parameters.
| Condition | Phase |
|---|---|
| Pregnancy Trimester, First Pregnancy Trimester, Second Pregnancy Trimester, Third | Phase I |
MedlinePlus consumer health information
Study Type: Observational
Study Design: Screening, Longitudinal, Defined Population, Prospective Study
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:
Expected Total Enrollment: 60
Study start: February 2006; Expected completion: December 2008
Last follow-up: June 2007; Data entry closure: June 2008
The subjects will be investigated as outpatients, for each subject 4 individual dates with a duration of approx. 30 min 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
Ages Eligible for Study: 20 Years - 42 Years, Genders Eligible for Study: Female
Accepts Healthy Volunteers
Criteria
Inclusion Criteria:
- · Eligibility: 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 concomittant disease
Location and Contact Information
Please refer to this study by ClinicalTrials.gov identifier NCT00180219
Joachim Siegert, MDDPharm,PhD +493514585694 joachim.siegert@tu-dresden.de
Germany
Medizinische Fakultät der Technischen Universität Dresden, Dresden, 01307, Germany
Joachim Siegert, MDDPharm,PhD +493514585694 joachim.siegert@tu-dresden.de
Study chairs or principal investigators
Joachim Siegert, MDDPharm,Phd, Principal Investigator, Technische Universität Dresden
More Information
Study ID Numbers: IKPD-S-01-04
Last Updated: September 15, 2005
Record first received: September 14, 2005
ClinicalTrials.gov Identifier: NCT00180219
Health Authority: Germany: Federal Institute for Drugs and Medicinal Devices
ClinicalTrials.gov processed this record on 2005-09-20
Last Updated: September 15, 2005
Record first received: September 14, 2005
ClinicalTrials.gov Identifier: NCT00180219
Health Authority: Germany: Federal Institute for Drugs and Medicinal Devices
ClinicalTrials.gov processed this record on 2005-09-20
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