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NCT01843517 · ClinicalTrials.gov registry record
Endogenous Pain Facilitation and Inhibition in Postpartum Women
A clinical trial, sponsored by Wake Forest University.
- Completed
- Registry status
- 80
- Enrollment target
NCT01843517 is a clinical trial that has completed, run by Wake Forest University. The registered enrollment target is 80 participants.
The verdict
NCT01843517 has completed, sponsored by Wake Forest University.
- COMPLETED
- Registry status
- 80 participants
- Enrollment target
Study Summary
This study seeks to further understand these three observations - (1) that the time period surrounding childbirth accelerates recovery from pain after injury (2) that this likely reflects dampened facilitating mechanisms and exaggerated inhibitory mechanisms, and (3) that stress may interfere with this protection. In this study the investigators will compare women within 2 weeks of delivery to age matched controls and anticipate that pain inhibition is increased after delivery, pain facilitation is decreased, and that there is a relationship between these pain responses and the degree of pre-existing stress.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 80 participants |
| Start Date | 2013-04 |
| Est. Completion | 2017-12-05 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01843517
The ClinicalTrials.gov registry entry for NCT01843517 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 80 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wake Forest University, which has 100 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 0 interventions.
NCT01843517 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01843517 about?
NCT01843517 is a clinical study titled "Endogenous Pain Facilitation and Inhibition in Postpartum Women". This study seeks to further understand these three observations - (1) that the time period surrounding childbirth accelerates recovery from pain after injury (2) that this likely reflects dampened facilitating mechanisms and exaggerated inhibitory mechanisms, and (3) that stress may interfere with t...
What is the current status of trial NCT01843517?
This trial is currently completed. The enrollment target is 80 participants. The study started on 2013-04. Estimated completion is 2017-12-05.
Who is sponsoring clinical trial NCT01843517?
This trial is sponsored by Wake Forest University, which has 100 total clinical trials registered on ClinicalTrials.gov.
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