Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
20 participants
OBSERVATIONAL
2015-12-31
2020-03-31
Brief Summary
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Detailed Description
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* Assessment via ultrasound measurement transabdominally
* 3 groups of participants: 1.) 20 pregnant women, who have never been pregnant before; 2.) 40 pregnant women with their first pregnancy, followed over the course of pregnancy; 3.) 20 women1-5 days after delivery (10 after spontaneous delivery, 10 after planned cesarean section)
* comparison between pregnant and non-pregnant women; evaluation of influence of pregnancy and mode of delivery
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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non-pregnant women
20 non-pregnant women, BMI \< 30 kg/m2, Nulligravidas, no abdominal pre-operations, aged 20-45 years, measurement of the abdominal muscles and interrectal distance by ultrasound
Ultrasound
ultrasound measures
pregnant women
40 pregnant women, BMI \< 30 kg/m2 before pregnancy, Primigravidas, no abdominal pre-operations, aged 20-45 years, measurement of the abdominal muscles and interrectal distance by ultrasound, consecutive measurement during the course of pregnancy
Ultrasound
ultrasound measures
women who deliverd
20 pregnant women, BMI \< 30 kg/m2 before pregnancy, Primiparas, no abdominal pre-operations, aged 20-45 years, measurement of the abdominal muscles and interrectal distance by ultrasound, measurement after delivery (10 after spontaneous delivery, 10 after elective cesarean section)
Ultrasound
ultrasound measures
Interventions
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Ultrasound
ultrasound measures
Eligibility Criteria
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Inclusion Criteria
* pregnant women aged 20-45 y with a BMI \< 30 kg/m2 before pregnancy
Exclusion Criteria
* chronical lung diseases
* constipation
* maternal collagenosis
* polyhydramnion (AFI \> 25)
* uterus fibroids \> 10 cm
* inability to perform Valsalva
20 Years
45 Years
FEMALE
Yes
Sponsors
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University of Zurich
OTHER
Responsible Party
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Principal Investigators
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Nina Kimmich, MD
Role: PRINCIPAL_INVESTIGATOR
University of Zurich
Locations
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University Hospital Zurich
Zurich, , Switzerland
Countries
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Other Identifiers
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KEK-ZH-Nr.2015-0008
Identifier Type: -
Identifier Source: org_study_id
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