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NCT03004872

Relationship Between Postpartum Mood Disorders and Delivery Experience

Completed Last updated 12 February 2019
What this trial tests

trial in Postpartum Period in 600 participants. Completed in 17 December 2018.

Timeline
31 October 2016
Primary endpoint
17 December 2018
17 December 2018

Quick facts

Lead sponsorUniversity of Michigan
StatusCompleted
Study typeOBSERVATIONAL
Enrollment600
Start date31 October 2016
Primary completion17 December 2018
Estimated completion17 December 2018
Sites1 location across United States

Conditions studied

Sponsor

University of Michigan

Who can join

18 and older, female only, with Postpartum Period or Depression. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. The associations of subjective appraisal of birth pain and provider-patient communication with postpartum-onset PTSD.
    Kountanis JA, Kirk R, Handelzalts JE, Jester JM, et al · · 2022 · cited 13× · PMID 34250546 · DOI 10.1007/s00737-021-01154-z

Verify or expand the search:

Other recruiting trials for Postpartum Period

Currently open trials in the same condition.

Other University of Michigan trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03004872.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing