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NCT04546204 Clinical Trial

COMPARISON OF OBSTETRIC AND NEONATAL OUTCOMES OF ADOLESCENT PREGNANCİES

Pregnancy Related Clinical Trial

Official title:
COMPARISON OF OBSTETRIC AND NEONATAL OUTCOMES BETWEEN SYRIAN ADOLESCENT REFUGEES AND LOCAL TURKISH ADOLESCENT CITIZENS.

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04546204
Other study ID # adolescentpregnancy
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 1, 2020
Est. completion date September 1, 2020

Study information
Verified date September 2020
Source Alkü Alanya Education and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

ABSTRACT

Adolescent pregnancy rates are gradually increasing in the recent decades. As a reason of war nutritional difficulties, language differences and difficulty in applying to the health institution causes lack of prenatal care. As a reason of absence of prenatal care, associated medical complications can occur. 525 adolescent women who gave birth to singletons agreed to participate in this study. Data on maternal demographic and obstetric characteristics as well as neonatal outcomes were analyzed. In conclusion, adolescent pregnancy continues to be an important social problem due to the health support needs. However, the results of our present study are important in terms of showing that the perinatal care is quietly improved in Turkey.

Recruitment information / eligibility
Status Completed
Enrollment 525
Est. completion date September 1, 2020
Est. primary completion date August 1, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 14 Years to 16 Years
Eligibility Inclusion Criteria:

- 14-16 y Age

Exclusion Criteria:

- over 16 years

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• vaginal delivery
normal vaginal spontaneous delivery

Locations
Country Name City State
Turkey Alkü Education and Research Hospital Antalya

Sponsors (1)
Lead Sponsor Collaborator
Alkü Alanya Education and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary vaginal delivery rate 2 years
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