Trials / Terminated
TerminatedNCT01181843
Incidence of Respiratory Depression in Cesarean Section
A Prospective, Observational, Double-blind (Black-Box) Study Evaluating Incidence, Severity and Predictive Factors of Respiratory Depression During Postoperative Neuraxial Opioid Analgesia in Obstetric Patients After Cesarean Delivery Using Current Standard Intermittent Postoperative Monitoring Compared to Continuous Pulse Oximetry / Capnography
- Status
- Terminated
- Phase
- —
- Study type
- Observational
- Enrollment
- 100 (actual)
- Sponsor
- Wake Forest University · Academic / Other
- Sex
- Female
- Age
- 18 Years – 55 Years
- Healthy volunteers
- Not accepted
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.
Conditions
Timeline
- Start date
- 2010-07-01
- Primary completion
- 2014-06-01
- Completion
- 2014-06-01
- First posted
- 2010-08-13
- Last updated
- 2017-11-08
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01181843. Inclusion in this directory is not an endorsement.