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Postpartum Depression Treatment Study

In this study, we want to see if a new medicine helps reduce symptoms of depression after childbirth. This is called postpartum depression. The sooner postpartum depression is treated, the faster the parent and baby can bond after birth.

Age & Gender

  • 18 years ~ 45 years
  • Female, Gender Inclusive

Visit Availability

  • Standard business hours (M-F, 8-5)
  • Extended hours (M-F, early morning or evening)

Location

North Carolina (Statewide)

What will be asked of you

This study includes visits to the clinic and some remote visits. We will check your vital signs, collect blood and urine samples, do a physical exam, and perform an EKG. You will also fill out questionnaires. The study involves taking medication as well.

Incentives

Up to $700 , Travel compensation and caregiver compensation available

In-person visits:
7
Phone or online visits:
4
Total length of participation:
1-2 months

Looking for Specific Volunteers

Able to participate:

  • You have given birth in the past 12 months
  • You are experiencing symptoms of low mood, sleep or appetite changes, anxiety, loss of interest in your normal activities

Not eligible if:

  • You have been treated with electroconvlusive therapy in the past 3 months
  • You have been diagnosed with postpartum psychosis, bipolar disorder, schizophrenia, or schizoaffective disorder

Contact the Team

Visit Location

Contact & Visit Location

Primary Contact

Primary Visit Location

Clinical and Translational Research Center (CTRC)
Burnett-Womack Building (UNC-Chapel Hill)
160 Dental Cir, Chapel Hill, NC 27514, USA

Additional Study Information

Principal Investigator

Morgan Patterson
Psychiatry - General

Study Type

Clinical or Medical
Interventional

Study Topics

Behavior
Mental and Emotional Health
Pregnancy
Sexual and/or Reproductive Health
Women's Health

IRB Number

24-1889

ClinicalTrials.gov

06342310

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