Clinical Trials Directory

Trials / Completed

CompletedNCT02933541

Central Arterial Pressure Changes With Use of Regional Anesthesia in Obstetric Patients

Status
Completed
Phase
Study type
Observational
Enrollment
12 (actual)
Sponsor
St. Louis University · Academic / Other
Sex
Female
Age
14 Years – 50 Years
Healthy volunteers
Accepted

Summary

Plan to monitor central arterial pressure in women who are undergoing spinal anesthesia for cesarean delivery or epidural anesthesia for vaginal delivery.

Detailed description

Subjects will be screened as they are admitted to the maternity care floor (5th floor St. Mary's Hospital). Subjects will be approached if they are desiring regional anesthesia. The subject will have an additional blood pressure cuff placed on the arm that anesthesia is not using for their blood pressure cuff. Central arterial pressure will be measured from the cuff: * Prior to regional anesthesia placement * Every 15 minutes for 1 hour * Every 30 minutes for 2 hours Routine sphygmomanometer measurements will also completed at the above times. These are all study procedures. Anesthesia will use their usual protocol for blood pressure monitoring and management during placement of, and after the procedure. No changes in patient management will be made based upon the central arterial pressure as the guidelines were developed with routine brachial pressure.

Conditions

Timeline

Start date
2016-09-01
Primary completion
2023-10-19
Completion
2023-10-19
First posted
2016-10-14
Last updated
2024-07-12

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02933541. Inclusion in this directory is not an endorsement.