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NCT01996592 · ClinicalTrials.gov registry record
Persistent Pain After CS Delivery
A clinical trial, sponsored by Wake Forest University Health Sciences.
- Completed
- Registry status
- 575
- Enrollment target
NCT01996592: Completed study, sponsored by Wake Forest University Health Sciences.
NCT01996592 is a clinical trial that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 575 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01996592 has completed, sponsored by Wake Forest University Health Sciences.
- COMPLETED
- Registry status
- 575 participants
- Enrollment target
Study Summary
Many factors influence the development of persistent pain after CS (chronic pain) as well as post-partum depression. We are attempting to use trajectory pain methods in an attempt to identify those at risk for the development of persistent pain post delivery using a daily method of contact for the determination of pain scores. Assessments are also done evaluating satisfaction of pain management and maternal/infant bonding opportunities. Physical activity is monitored by subject's wearing a Fitbit with correlation being done with pain scores obtained over 60 days postop with eligible subjects..
Primary Outcome
By identifying preoperative risk factors for chronic pain and mapping out the trajectory of pain after cesarean delivery, we may be able to use novel pharmacologic or psychological interventions to alter postoperative pain trajectories. Two predominant risk factors have been determined thus far to put those at risk. They are emotional distress/depression and perceived stress. The 530 participants recovery pain scores were broken down into 3 subgroups--group 1 is those who had the fastest recover
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 575 participants |
| Start Date | 2013-05 |
| Est. Completion | 2016-01 |
What the finished NCT01996592 record still lists
NCT01996592 is an observational study that tracks outcomes without assigning an intervention. The registered 575 participants enrollment target is mid-sized for trials with a published cap.
The record links to 0 conditions, and to 0 interventions.
NCT01996592 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01996592 about?
NCT01996592 is a clinical study titled "Persistent Pain After CS Delivery". Many factors influence the development of persistent pain after CS (chronic pain) as well as post-partum depression. We are attempting to use trajectory pain methods in an attempt to identify those at risk for the development of persistent pain post delivery using a daily method of contact for the d...
What is the current status of trial NCT01996592?
This trial is currently completed. The enrollment target is 575 participants. The study started on 2013-05. Estimated completion is 2016-01.
Who is sponsoring clinical trial NCT01996592?
This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.
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