- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03232294
Fetal Front-abdominal Wall Thickness and Perinatal Outcome
Effect of Fetal Front-abdominal Wall Thickness on Birth Weight and Perinatal Outcome at 24-26. Gestational Weeks
Study Overview
Status
Study Type
Enrollment (Actual)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
A total of 96 women with low risk pregnancy coming to our clinic for a routine antenatal examination in 26-28th gestational weeks were included to this study and performed 75 gr- oral glucose tolerance test (OGTT).
Exclusion Criteria:
The participants with a positive 75-g OGTT were excluded. Additionally those following criteria were accepted as the exclusion criteria of this study: hypertension, preeclampsia, diabetes, fetal distress, fetal anomaly, multiple pregnancy, preterm labor, preterm premature rupture of membrane, placenta previa, polyhydramnios and intrauterine fetal growth restriction.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
---|
the study group
A total of 96 women with low risk pregnancy coming to the clinic for a routine antenatal examination in 26-28th gestational weeks were included to this study
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
The relationship between fetal abdominal wall thickness and macrosomia
Time Frame: 6 months
|
6 months
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2017/222
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Fetal Macrosomia
-
The First Affiliated Hospital with Nanjing Medical...Not yet recruiting
-
The University of Texas Health Science Center,...WithdrawnMacrosomia, Fetal | Retardation, Fetal Growth
-
The University of Texas Health Science Center,...Harris Health System, Lyndon B Johnson Hospital obstetrics and gynecology...WithdrawnLabor Induction | Macrosomia, Fetal
-
University of Modena and Reggio EmiliaTerminatedMacrosomia, Fetal | Large for Gestational Age BabyItaly
-
Peking University First HospitalCompletedDiabetes | Gestational Diabetes | Macrosomia, Fetal
-
The University of Texas Health Science Center,...Recruiting
-
Cairo UniversityRecruitingGestational Diabetes | IUGR | Pre-Gestational Diabetes | Macrosomia, FetalEgypt
-
Tufts Medical CenterEunice Kennedy Shriver National Institute of Child Health and Human Development... and other collaboratorsActive, not recruitingObesity | Lifestyle-related Condition | Macrosomia, FetalUnited States
-
Hospices Civils de LyonActive, not recruitingBirth Weight | Macrosomia, FetalFrance
-
CHU de ReimsUnknown