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NCT01298778 · ClinicalTrials.gov registry record · NA
High Pain Intervention in Cesarean Sections
A NA study, sponsored by Wake Forest University Health Sciences.
- Completed
- Registry status
- NA
- Development phase
- 69
- Enrollment target
NCT01298778 is a NA study that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 69 participants.
The verdict
NCT01298778, a NA study, has completed, sponsored by Wake Forest University Health Sciences.
- COMPLETED
- Registry status
- NA
- Development phase
- 69 participants
- Enrollment target
Study Summary
In previous studies the investigators have seen that the severity of pain one day after cesarean delivery can predict the presence of pain and depression 2 months later. The investigators believe those at risk for severe acute post-partum pain can be identified, and medical interventions can be tailored to manage postoperative pain more effectively.
Interventions
- DRUG Acetaminophen
- DRUG Duramorph 150
- DRUG Duramorph 300
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 69 participants |
| Start Date | 2010-08 |
| Est. Completion | 2011-07 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01298778
The ClinicalTrials.gov registry entry for NCT01298778 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 69 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 3 interventions - of which Acetaminophen is the first listed.
NCT01298778 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01298778 about?
NCT01298778 is a clinical study titled "High Pain Intervention in Cesarean Sections". In previous studies the investigators have seen that the severity of pain one day after cesarean delivery can predict the presence of pain and depression 2 months later. The investigators believe those at risk for severe acute post-partum pain can be identified, and medical interventions can be tail...
What is the current status of trial NCT01298778?
This trial is currently completed. It is a NA study. The enrollment target is 69 participants. The study started on 2010-08. Estimated completion is 2011-07.
What interventions are being tested in trial NCT01298778?
The interventions under investigation include: Acetaminophen (DRUG), Duramorph 150 (DRUG), Duramorph 300 (DRUG).
Who is sponsoring clinical trial NCT01298778?
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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