Postpartum Depression Clinical Trials

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Perinatal Thymic Dysregulation: Characterization of Perinatal Mood Episodes

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The perinatal period is recognized as a time of heightened psychological vulnerability. This research aims to improve the diagnosis and therapeutic management of mood episodes occurring during this time. It is integrated into routine clinical care and seeks to standardize the evaluation of criteria used to characterize mood episodes, while also exploring relevant contextual factors. Traditionally, clinical attention has focused on postnatal depression; however, increasing evidence highlights the presence of hypomanic symptoms-such as distractibility, reduced need for sleep, tachypsychia, and irritability-during the postpartum period. These symptoms may coexist with depressive features, resulting in complex clinical presentations that are often difficult to recognize and manage. Consequently, many cases go undiagnosed and untreated. Current research has largely concentrated on depressive episodes (perinatal depression), with less emphasis on manic, hypomanic, or mixed episodes indicative of bipolar disorder. A systematic evaluation of hypomanic symptoms occurring alongside depressive symptoms in the postpartum period could refine clinical diagnosis and support more targeted and effective therapeutic interventions.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• Women over 18 years old

• Pregnant or having given birth less than a year ago

• First psychiatric consultation for the pregnancy concerned.

• Good command of the French language.

• Participant affiliated to the social security system

• Participant who has given her consent to take part in the study.

Locations
Other Locations
France
Centre Hospitalier CHARLES PERRENS
RECRUITING
Bordeaux
Contact Information
Primary
Anne-Laure SUTTER DALLAY, Prof, MD, PhD
alsutter@ch-perrens.fr
+33 556561782
Backup
Helen SAVARIEAU
hsavarieau@ch-perrens.fr
+33556563556
Time Frame
Start Date: 2025-10-13
Estimated Completion Date: 2026-12-31
Participants
Target number of participants: 200
Treatments
Experimental: Usual care
The study aims to systematize the evaluation of the various criteria used to characterize mood episodes, and to explore contextual elements.
Sponsors
Leads: Centre Hospitalier Charles Perrens, Bordeaux

This content was sourced from clinicaltrials.gov