Clinical Trials Directory

Trials / Completed

CompletedNCT03004872

Relationship Between Postpartum Mood Disorders and Delivery Experience

Status
Completed
Phase
Study type
Observational
Enrollment
600 (actual)
Sponsor
University of Michigan · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate potential risk factors for developing postpartum depression or posttraumatic stress disorder during the first year postpartum in patients who have no preexisting history of PTSD or PPD.

Detailed description

It is theorized that poor pain control during labor and cesarean delivery, non-elective inductions, unplanned surgeries such as urgent/emergent cesarean delivery or operating room management of postpartum hemorrhage, and opioid abuse/addiction are risk factors for developing postpartum depression (PPD) or post-traumatic stress disorder (PTSD) after delivery. This study will, through questionnaires, interviews, and examination of the medical record, seek to identify whether and how strongly such correlations exist during the first year postpartum in patients who have no preexisting history of these conditions.

Conditions

Timeline

Start date
2016-10-31
Primary completion
2018-12-17
Completion
2018-12-17
First posted
2016-12-29
Last updated
2019-02-12

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03004872. Inclusion in this directory is not an endorsement.