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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04427410
Other study ID # TYL-2019-12476
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 20, 2019
Est. completion date February 20, 2020

Study information

Verified date June 2020
Source Cukurova University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

There are studies in the literature that associate oxytocin level with postpartum depression. This study was carried out to investigate the relationship between oxytocin levels measured during pregnancy and postpartum depression symptoms.


Description:

Introduction and purpose: There are studies in the literature that associate oxytocin level with postpartum depression. This study was carried out to investigate the relationship between oxytocin levels measured during pregnancy and postpartum depression symptoms.

Method: The study was conducted with 70 women who met the research criteria. Data collection was done in two interviews. The first meeting is 30-38 at the week of gestation, the second interview is 4-12 at the week of postpartum. It was done between weeks. In each interview, a data collection form was applied first and then a saliva sample was taken. Data collection form; The questions prepared by the researchers consisted of the Edinburgh Postnatal Depression Scale (EPDS) and Beck Depression Inventory (BDI). The data were analyzed using SPSS 22.0 program and the significance value was taken as p <0.05.


Recruitment information / eligibility

Status Completed
Enrollment 70
Est. completion date February 20, 2020
Est. primary completion date October 20, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- 18 years of age or older, and having a pregnancy of 30 weeks or more

Exclusion Criteria:

- previous mental illness history, miscarriage or stillbirth history, multiple pregnancy, fetal malformation, antidepressant or anxiolytic drug use, existing chronic disease,preterm labor is the development of maternal or neonatal complications at birth, hospitalization in the neonatal intensive care unit or congenital disease.

Study Design


Intervention

Diagnostic Test:
Salivary test
Salivary test for measured of oxytocin levels

Locations

Country Name City State
Turkey Cukurova University Adana Saricam

Sponsors (2)

Lead Sponsor Collaborator
Cukurova University Ayseren Cevik

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Oxytocin levels Oxytocin levels in pregnancy and postpartum period 3-6 month
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