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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 is a clinical trial that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 575 participants.
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..
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 575 participants |
| Start Date | 2013-05 |
| Est. Completion | 2016-01 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01996592
The ClinicalTrials.gov registry entry for NCT01996592 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 575 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wake Forest University Health Sciences, which has 1,140 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 0 interventions.
NCT01996592 reports 0 study locations.
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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