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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00872313
Other study ID # NMU-200903-MZ003
Secondary ID NJFY09102M107
Status Completed
Phase N/A
First received March 30, 2009
Last updated January 11, 2014
Start date February 2009
Est. completion date August 2012

Study information

Verified date January 2014
Source Nanjing Medical University
Contact n/a
Is FDA regulated No
Health authority China: Ethics Committee
Study type Observational

Clinical Trial Summary

A range of psychological disorders occur in women in the postpartum period. These include "the blues", which occurs in the first days after birth and which is very common and self-limiting; severe psychoses often associated with mania or bipolar illness, occurring in the first weeks after birth; and mild to moderate depression, occurring weeks to months after birth. Studies have been done focused on postpartum psychosis using a retrospective investigation, which gave only a limited material on the prevalence of psychological disorders in postpartum women. The investigators hypothesized that different pathways to psychosis function as the risk factors which may be overlapped, truly independent, mediating, or moderating, in new mothers who are at high risk and/or during the early period of delivery. In addition, the investigators purposed that the temporal sequence of biological, social and demographic variables are also the potential factors contributing to the development of postpartum psychosis.


Recruitment information / eligibility

Status Completed
Enrollment 4000
Est. completion date August 2012
Est. primary completion date August 2012
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- Pregnant women

- Chinese

Exclusion Criteria:

- Age < 18 years or > 50 years

- Gestational age < 32 weeks

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Locations

Country Name City State
China Nanjing Maternal and Child Health Care Hospital Nanjing Jiangsu

Sponsors (1)

Lead Sponsor Collaborator
Nanjing Medical University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of psychoses 3 months and 6 months postpartum Yes
Secondary Antepartum economic level One year before labor and delivery (recorded by antepartum communication) No
Secondary Antepartum social status One year before labor and delivery (recorded by antepartum communication) No
Secondary Antepartum psychological level 1 day before birth No
Secondary Intrapartum complications 1 day after birth Yes
Secondary Baby characteristics One minute, 5min, 15min after baby was born No
Secondary Maternal characteristics One day after birth Yes
Secondary Medical caregiver characteristics One day before and after the labor completion No
Secondary Parturient family characteristics One week before labor and delivery, recorded by investigators through patients' antepartum communication No
Secondary Intrapartum medical procedures One day after birth Yes
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