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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: Clinical Trial study, sponsored by Wake Forest University.
NCT01181843 is a clinical trial that was terminated before completion, run by Wake Forest University. The registered enrollment target is 100 participants. According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
RESPIRATORY DEPRESSION OBSERVATION ONLY OF CURRENT PRACTICES, DOES NOT INVOLVE TREATMENT
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2010-07 |
| Est. Completion | 2014-06 |
Why NCT01181843 stopped before completion
NCT01181843 is an observational study that tracks outcomes without assigning an intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap.
The record links to 0 conditions, and to 0 interventions.
NCT01181843 does not publish any study locations in the registry export this page uses.
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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