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Trial record 36 of 256 for:    postpartum | "Depression"

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

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ClinicalTrials.gov Identifier: NCT02682004
Recruitment Status : Unknown
Verified February 2016 by Mehmet Baki Senturk, Zeynep Kamil Maternity and Pediatric Research and Training Hospital.
Recruitment status was:  Recruiting
First Posted : February 15, 2016
Last Update Posted : February 15, 2016
Sponsor:
Information provided by (Responsible Party):
Mehmet Baki Senturk, Zeynep Kamil Maternity and Pediatric Research and Training Hospital

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.

Condition or disease Intervention/treatment
Postpartum Depression Other: leptin, serotonin and adiponectin level Other: leptin,serotonin, adiponectin level

Study Type : Observational
Estimated Enrollment : 400 participants
Observational Model: Case Control
Time Perspective: Prospective
Official Title: Serotonin, Leptin and Adiponectin Level in Patients With Postpartum Depression: Controlled Study
Study Start Date : February 2016
Estimated Primary Completion Date : April 2016
Estimated Study Completion Date : May 2016

Resource links provided by the National Library of Medicine

Drug Information available for: Serotonin

Group/Cohort Intervention/treatment
Women with postpartum depression Other: leptin, serotonin and adiponectin level
Women without postpartum depression Other: leptin,serotonin, adiponectin level



Primary Outcome Measures :
  1. Blood level (ng/ml) ELİSA [ Time Frame: 1 month ]


Information from the National Library of Medicine

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Ages Eligible for Study:   20 Years to 40 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population
According to Edinburg depression scale womenn who taken 13 point and above.
Criteria

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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02682004


Contacts
Contact: Mehmet Baki Şentürk, MD +905417737176 dr.baki77@gmail.com

Locations
Turkey
Zeynep Kamil Maternity and Pediatric Research and Training Hospital Recruiting
İstanbul, Turkey, 34668
Sponsors and Collaborators
Zeynep Kamil Maternity and Pediatric Research and Training Hospital

Additional Information:
Publications of Results:
Responsible Party: Mehmet Baki Senturk, Principal investigator, Zeynep Kamil Maternity and Pediatric Research and Training Hospital
ClinicalTrials.gov Identifier: NCT02682004     History of Changes
Other Study ID Numbers: 51
First Posted: February 15, 2016    Key Record Dates
Last Update Posted: February 15, 2016
Last Verified: February 2016

Additional relevant MeSH terms:
Depression
Depressive Disorder
Depression, Postpartum
Puerperal Disorders
Behavioral Symptoms
Mood Disorders
Mental Disorders
Pregnancy Complications
Serotonin
Serotonin Receptor Agonists
Serotonin Agents
Neurotransmitter Agents
Molecular Mechanisms of Pharmacological Action
Physiological Effects of Drugs