Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT07008183

Perinatal Thymic DYsregulation: Characterization of Perinatal Mood Episodes

Led by Centre Hospitalier Charles Perrens, Bordeaux · Updated on 2025-12-01

200

Participants Needed

1

Research Sites

63 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Perinatal Thymic DYsregulation: Characterization of Perinatal Mood Episodes

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • 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
Not Eligible

You will not qualify if you...

  • Women who gave birth more than a year ago
  • Participant under psychiatric care
  • Participant under court protection

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Centre Hospitalier CHARLES PERRENS

Bordeaux, New Aquitaine, France, 33076

Actively Recruiting

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Research Team

A

Anne-Laure SUTTER DALLAY, Prof, MD, PhD

CONTACT

H

Helen SAVARIEAU

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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Perinatal Thymic DYsregulation: Characterization of Perinatal Mood Episodes | DecenTrialz