Postpartum Depression

NCT ID: NCT04278456

Last Updated: 2020-02-20

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Total Enrollment

300 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-03-21

Study Completion Date

2020-07-21

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Our aim was to diagnose and initiate early treatment for postpartum depression by detecting the changes of melatonin levels in c-sections with different antesthesia modalities.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Postpartum Depression Melatonin

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

general anesthesia

c-section with general anesthesia

postpartum depression

Intervention Type BEHAVIORAL

melatonin levels in c-sections with different anesthesia modalities.

spinal anesthesia

c-section with spinal anesthesia

postpartum depression

Intervention Type BEHAVIORAL

melatonin levels in c-sections with different anesthesia modalities.

epidural anesthesia

c-section with epidural anesthesia

postpartum depression

Intervention Type BEHAVIORAL

melatonin levels in c-sections with different anesthesia modalities.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

postpartum depression

melatonin levels in c-sections with different anesthesia modalities.

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* pregnant women c-section (using general or regional anesthesia) aged between 18-45 years

Exclusion Criteria

* age under 18 or above 45, history of smoking, a diagnosis with mental retardation, psychiatric patients, use of antipsychotics or antidepressants, patients with sleeping disorders, hormone replacement theraphy patients.
Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Erzincan University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

REMZIYE AYSENUR NALBANT

MD

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Remziye Ayşenur NALBANT

Role: PRINCIPAL_INVESTIGATOR

ERZİNCAN

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Erzincan Byu

Erzincan, , Turkey (Türkiye)

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Turkey (Türkiye)

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

DİDEM ONK

Role: CONTACT

05053856322

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

DİDEM ONK

Role: primary

05053856322

References

Explore related publications, articles, or registry entries linked to this study.

Andersen LP, Werner MU, Rosenberg J, Gogenur I. A systematic review of peri-operative melatonin. Anaesthesia. 2014 Oct;69(10):1163-71. doi: 10.1111/anae.12717. Epub 2014 May 19.

Reference Type RESULT
PMID: 24835540 (View on PubMed)

Maitra S, Baidya DK, Khanna P. Melatonin in perioperative medicine: Current perspective. Saudi J Anaesth. 2013 Jul;7(3):315-21. doi: 10.4103/1658-354X.115316.

Reference Type RESULT
PMID: 24015137 (View on PubMed)

Dianatkhah M, Ghaeli P, Hajhossein Talasaz A, Karimi A, Salehiomran A, Bina P, Jalali A, Ghaffary S, Shahmansouri N, Vejdani S. Evaluating the Potential Effect of Melatonin on the post-Cardiac Surgery Sleep Disorder. J Tehran Heart Cent. 2015 Jul 3;10(3):122-8.

Reference Type RESULT
PMID: 26697084 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

EBYU 88

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.