Ignite Creation Date:
2024-05-06 @ 9:37 AM
Last Modification Date:
2024-10-26 @ 12:16 PM
Study NCT ID:
NCT03022526
Status:
COMPLETED
Last Update Posted:
2020-08-19
First Post:
2017-01-11
Brief Title:
CSE v Epidural for Postpartum Depression
Sponsor:
Grace Lim MD MS
Organization:
University of Pittsburgh
Study Overview
Official Title:
Combined Spinal Epidural v Epidural Labor Analgesia for Postpartum Depression Symptoms COPE Trial Pilot Randomized Control Trial
Status:
COMPLETED
Status Verified Date:
2020-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
COPE
Brief Summary:
The purpose of this pilot prospective randomized control trial is to compare the initiation of labor epidural analgesia by combined spinal epidural vs epidural for the influence on risk for postpartum depression symptoms Investigators will randomize women to the receipt of CSE or E during labor after measuring baseline psychological psychosocial and psychophysical factors related to pain and depression The immediate research goals are to understand whether the association between labor pain and PPD is modifiable through the use of tailored anesthetic techniques
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None