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NCT01181843 · ClinicalTrials.gov registry record
Incidence of Respiratory Depression in Cesarean Section
A clinical trial, sponsored by Wake Forest University.
- Terminated
- Registry status
- 100
- Enrollment target
NCT01181843 is a clinical trial that was terminated before completion, run by Wake Forest University. The registered enrollment target is 100 participants.
The verdict
NCT01181843 was terminated before completion, sponsored by Wake Forest University.
- TERMINATED
- Registry status
- 100 participants
- Enrollment target
Study Summary
This study is designed to determine the incidence and severity of respiratory depression in elective cesarean section patients who have received a spinal or epidural narcotic called duramorph for management of postoperative pain. A monitoring device called a capnograph as well as a device called a pulse oximeter is placed on the patient once in the recovery room after delivery. The capnograph monitors the carbon dioxide level that the patient breathes out as well as their respiratory rate. The pulse oximeter is a device that is taped on the patient's finger and measures their oxygen saturation level. The monitoring is maintained for 18-24 hours after surgery.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2010-07 |
| Est. Completion | 2014-06 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01181843
The ClinicalTrials.gov registry entry for NCT01181843 describes a study currently listed as terminated, categorized as an unspecified phase. The registered enrollment target is 100 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.
NCT01181843 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01181843 about?
NCT01181843 is a clinical study titled "Incidence of Respiratory Depression in Cesarean Section". This study is designed to determine the incidence and severity of respiratory depression in elective cesarean section patients who have received a spinal or epidural narcotic called duramorph for management of postoperative pain. A monitoring device called a capnograph as well as a device called a p...
What is the current status of trial NCT01181843?
This trial is currently terminated. The enrollment target is 100 participants. The study started on 2010-07. Estimated completion is 2014-06.
Who is sponsoring clinical trial NCT01181843?
This trial is sponsored by Wake Forest University, which has 100 total clinical trials registered on ClinicalTrials.gov.
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