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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03251794
Other study ID # FAGE
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 1, 2017
Est. completion date April 18, 2018

Study information

Verified date June 2018
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Preterm birth continues to be a major public health problem with lasting family and societal repercussions. Despite tremendous research effort, prevention strategies have failed, and the prevalence of preterm birth in the United States reached 12.3% in 2003.

Prematurity causes 70% of fetal/neonatal deaths. 11.4% of births are at < 37 weeks' gestation. The rate of prematurity increases dramatically with the number of fetuses - singletons 10%; twins 54.9%; and triplets 93.6%


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date April 18, 2018
Est. primary completion date March 15, 2018
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

1. singleton fetus less than 37 weeks of gestation

2. women diagnosed to having Threatened preterm labor.

1. presence of uterine contraction (at least 4 in 20 min or 8 in 60 min )

2. cervical effacement <80 %

3. cervical dilatation <1 cm

Exclusion Criteria:

1. suspected fetal growth restriction,

2. maternal medical complications,

3. presence of fetal heart rate abnormalities at enrollment.

4. Preterm Premature rupture of membranes

5. Placenta previa

6. Lower urinary tract infection or genital infection

7. Fetal congenital anomaly

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
three dimensional ultrasound
evaluation of the suprarenal glands
color Doppler
Doppler evaluation of the suprarenal artery

Locations

Country Name City State
Egypt Assiut Faculty of Medicine Assiut

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary the volume of adrenal gland measurement by three dimensional ultrasound 5 minutes
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