NCT02682004CompletedNot Applicable
Serotonin, Leptin and Adiponectin Level in Patients With Postpartum Depression: Controlled Study
Zeynep Kamil Maternity and Pediatric Research and Training Hospital1 site in 1 country400 target enrollmentStarted: February 2016Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 400
- Locations
- 1
- Primary Endpoint
- Blood level (ng/ml) ELİSA
Study Overview
Brief Summary
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.
Study Design
- Study Type
- Observational
- Observational Model
- Case Control
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 20 Years to 40 Years (Adult)
- Sex
- Female
- Accepts Healthy Volunteers
- Yes
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
Outcomes
Primary Outcomes
Blood level (ng/ml) ELİSA
Time Frame: 1 month
Secondary Outcomes
No secondary outcomes reported
Investigators
Mehmet Baki Senturk
Principal investigator
Zeynep Kamil Maternity and Pediatric Research and Training Hospital
Study Sites (1)
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