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.