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Clinical trial

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

NCT01181843 is registered in ClinicalTrials.gov with Wake Forest University as lead sponsor.

NCT NCT01181843
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Registry record

As filed in ClinicalTrials.gov.

Title
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
Lead sponsor
Wake Forest University
Phase
Observational
Overall status
Terminated
Start date
July 31, 2010
Completion date
June 30, 2014
Enrollment
100 (actual)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

postoperative pain, respiratory depression