Serotonin, Leptin and Adiponectin Level in Patients With Postpartum Depression: Controlled Study

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

400 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-02-29

Study Completion Date

2017-05-31

Brief Summary

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After vaginal delivery, all of the participants will evaluate by using Edinburg depression scale and venous blood sample will obtain. Postpartum depression will consider the result of scale 13 and above according to Turkhish translate. Then leptin, adiponectin and serotonin level will compare between depressed and nondepressed women.

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Detailed Description

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Conditions

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Postpartum Depression

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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Women with postpartum depression

leptin, serotonin and adiponectin level

Intervention Type OTHER

Women without postpartum depression

leptin,serotonin, adiponectin level

Intervention Type OTHER

Interventions

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leptin, serotonin and adiponectin level

Intervention Type OTHER

leptin,serotonin, adiponectin level

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* All women who gave birth

Exclusion Criteria

* women with previously diagnosed depression and any psychiatric disorders
* women with previously take antidepressan and antipshycothic
* women giving birth to children with anomalies
* women with undertake surgery for peripartum hemorrhage

Minimum Eligible Age

20 Years

Maximum Eligible Age

40 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes