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Postpartum Depression clinical trials

View clinical trials related to Postpartum Depression.

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NCT ID: NCT05693792 Withdrawn - Clinical trials for Postpartum Depression

A Six-Month Prospective Follow-Up Study of WB001

Start date: February 1, 2023
Phase:
Study type: Observational

This study is a 6-month follow-up study to WB001-001 conducted to assess and evaluate the durability of the effect of {WB001+TAU} beyond the 8-week treatment period.

NCT ID: NCT04273191 Withdrawn - Clinical trials for Postpartum Depression

A Study to Evaluate Multimodal Neuroimaging Parameters in Women With Postpartum Depression Who Are Receiving ZULRESSO™ (Brexanolone)

Start date: February 2020
Phase: Phase 4
Study type: Interventional

In this Phase 4 study, women who have been prescribed commercial ZULRESSO™ (brexanolone) by a physician as standard of care for postpartum depression (PPD) and who are planning to receive the infusion per United States Prescribing Information (USPI) at a Risk Evaluation and Mitigation Strategy (REMS)-certified healthcare center are being asked to participate to collect data on multimodal neuroimaging parameters in order to evaluate the relationship between changes in depressive symptoms and changes in neuroimaging parameters.

NCT ID: NCT03949465 Withdrawn - Clinical trials for Postpartum Depression

rTMS for Peripartum Depression

Start date: May 18, 2023
Phase: N/A
Study type: Interventional

Repetitive Transcranial Magnetic Stimulation (rTMS) is a neuromodulatory technique that is effective in major depression. There is preliminary evidence suggesting that rTMS is effective in peripartum depression as well, however this comes from a number of very small studies. The objective is to study the effectiveness of rTMS in peripartum depression. The investigators will do so using an open label design in which participants will receive rTMS for four weeks. The focus is on clinical improvement in depressive symptoms; however the investigators will also look at other aspects such as perinatal anxiety and maternal-infant bonding as measured by self-report questionnaires.

NCT ID: NCT03709004 Withdrawn - Breastfeeding Clinical Trials

Pacifiers and Breastfeeding Among Mothers at Risk for Postpartum Depression

Start date: September 25, 2019
Phase: N/A
Study type: Interventional

We will enroll 40 mother-infant dyads in a randomized trial exploring the effect of distribution of pacifiers during the birth hospitalization to mothers at high risk for postpartum depression on pacifier use, infant feeding, and maternal stress.

NCT ID: NCT01909167 Withdrawn - Anxiety Clinical Trials

Keeping Well:Online Cognitive Behavioral Therapy (CBT) for Pregnant Women With Depressive Symptoms

OnCBTDep
Start date: June 1, 2020
Phase: N/A
Study type: Interventional

Most depression during pregnancy is undetected and untreated although it is known to be harmful both to the woman herself and her future child. When these mental disorders are detected, psychotherapies remain difficult to access, especially in primary care, despite being effective.Also, prenatal depression is known to be a strong risk factor for postnatal depression and may prejudice the mother-infant relationship. This leads us to the following question: Will individual Cognitive Behavioral Therapy (CBT) delivered online be a more effective treatment for symptoms of depression in pregnant women, than treatment as usual (TAU)? The proposed randomized controlled trial aims at evaluating the efficacy of internet based cognitive behavioural therapy(CBT) delivered individually via "skype", using video and audio resources, by a fully trained psychotherapist, compared to treatment as usual, in women suffering from symptoms of depression in pregnancy. Hypothesis The internet based interventions will be more effective at reducing symptoms of depression in pregnant women than treatment as usual, in terms of rates of diagnoses and levels of self rated symptoms of depression.

NCT ID: NCT00617045 Withdrawn - Clinical trials for Major Depressive Disorder

Duloxetine for the Treatment of Postpartum Depression

DuloxPPD
Start date: July 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to assess whether the antidepressant, duloxetine, is equally effective as a treatment for subjects who have a Postpartum Onset Depression compared to subjects who have an onset of Major Depressive Disorder prior to delivery. The hypothesis is that duloxetine will be as effective in subjects with Postpartum Major Depressive Disorder as in subjects with a Major Depressive Disorder.