OSA Screen Negative With Spinal Duramorph

Wake Forest University (WFU)

Status: Terminated

Conditions: Respiratory Depression

Treatments: Device: Capnography monitoring

Study type: Interventional

Funder types: Other

Identifiers

NCT03151226

IRB00033095

Details and patient eligibility

About

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.

Enrollment: 3 patients

Sex: Female

Ages: 18 to 50 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• 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

Exclusion criteria

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

Trial design

Primary purpose: Health Services Research

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

---

3 participants in 1 patient group

capnography monitoring

Other group

Description:

single arm, all subjects receiving duramorph will receive capnography monitoring

Treatment:

Device: Capnography monitoring