Evaluation of a Respiratory Monitor in Surgical Patients With a BMI>35

CompletedOBSERVATIONAL
Enrollment

90

Participants

Timeline

Start Date

February 28, 2013

Primary Completion Date

April 30, 2024

Study Completion Date

April 30, 2024

Conditions
ObesityObstructive Sleep Apnea
Interventions
DEVICE

ExSpiron Respiratory Volume Monitor (RVM, ExSpiron™, Respiratory Motion, Inc.; Waltham, MA

Monitoring sensors will be applied to patient's right chest and the monitoring device will collect breathing parameters such as breathing rate and volumes before, during and after the procedure until patient is ready to leave the recovery room. At the beginning and at the end of the study investigator will perform a one-time measurement of patient's respiratory parameters using a standard handheld spirometer. This is a non-invasive device that is commonly used in clinical care not related to research.

Trial Locations (1)

02111

Tufts Medical Center, Boston

All Listed Sponsors
lead

Tufts Medical Center

OTHER

NCT01825278 - Evaluation of a Respiratory Monitor in Surgical Patients With a BMI>35 | Biotech Hunter | Biotech Hunter