Clinical Trials Directory

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.

Incidence of Respiratory Depression in Cesarean Section (NCT01181843) · Clinical Trials Directory