OSA Screen Negative With Spinal Duramorph

Stopped early · Not applicable

Conditions studied: Respiratory Depression

In brief

Non emergent scheduled cesarean sections will be consented to participate in this study of patients who have screened negative for obstructive sleep apnea and who are also BMI\>/= 35 to have capnography monitoring postoperatively. The capnography and pulse oximetry will be initiated in the post anesthesia care unit and be worn for 12-24 hours after delivery. Data will be retrieved after that time period in a deidentified fashion. Medication usage will be reviewed as well as the standard of care information from the duramorph monitoring will be retrieved.

Key facts

Study ID

NCT03151226

Run by

Wake Forest University Health Sciences

People needed

3

Starts

2015-08-03

Expected to finish

2015-10-01

Last updated by the study team

2018-09-07

Who can join

Age: 18 and older, up to 50. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• OSA screen negative per hospital protocol
• age 18 or greater
• BMI>35
• consent to participate to wear capnography and pulse oximetry monitoring devices post delivery

You may not qualify if…

• Spanish speaking only
• under age 18
• contraindication to receiving drugs utilized in delivery anesthetic

Where it is running

• Novant Health Forsyth Medical Center — Winston-Salem, North Carolina, United States

Full record on ClinicalTrials.gov

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