Preeclampsia Clinical Trial
— RedCarRiskOfficial title:
Evaluation of Practicability in Survey and Test Procedures and of Successful Implementation of Complex Interventions - Feasibility Analysis Based on a Pilot Study: Influence of Conditional Workout Postpartum on Arterial Stiffness Among Women With Status After Preeclampsia, Superimposed Preeclampsia or HELLP-syndrome
NCT number | NCT02754778 |
Other study ID # | RedCarRisk-Study |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | April 2016 |
Est. completion date | March 2021 |
Verified date | March 2023 |
Source | Martin-Luther-Universität Halle-Wittenberg |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Evaluation of practicability in survey and test procedures and of successful implementation of complex interventions - feasibility analysis based on a pilot study: Influence of conditional workout postpartum on arterial stiffness among women with status after preeclampsia, superimposed preeclampsia or HELLP-syndrome
Status | Completed |
Enrollment | 40 |
Est. completion date | March 2021 |
Est. primary completion date | April 2019 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 40 Years |
Eligibility | Inclusion Criteria: - diagnosis of preeclampsia, superimposed gestosis or HELLP syndrome - capacity for content Exclusion Criteria: - eclamptic stroke - New York Heart Association > Stadium II - severe neurological or orthopedic disabilities - peripheral arterial occlusive disease - severe disease of the newborn which leads to an intensive familial care |
Country | Name | City | State |
---|---|---|---|
Germany | Maternity Clinic/Perinatal Treatment Center, Halle university hospital, Martin-Luther-Universität Halle-Wittenberg | Halle (Saale) | Sachsen Anhalt |
Germany | St. Elisabeth and St. Barbara Hospital / Women's clinic | Halle (Saale) | Saint |
Lead Sponsor | Collaborator |
---|---|
Martin-Luther-Universität Halle-Wittenberg |
Germany,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | reduced aortic pulse wave velocity by 1m/s | six month | ||
Secondary | no arterial hypertension defined as blood pressure =140mmHg / 80mmHg without antihypertensic medication | 13 years |
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