Status:
COMPLETED
Evaluation of a Respiratory Monitor in Surgical Patients With a BMI>35
Lead Sponsor:
Tufts Medical Center
Conditions:
Obesity
Obstructive Sleep Apnea
Eligibility:
All Genders
18+ years
Brief Summary
This study proposes to evaluate the clinical applicability of the ExSpiron Respiratory Volume Monitor (RVM, ExSpiron™, Respiratory Motion, Inc.; Waltham, MA) in obese surgical patients undergoing gene...
Eligibility Criteria
Inclusion
- ASA 1 - 3 patients with a body mass index (BMI) ≥ 35kg/m2 presenting for elective surgery under general anesthesia aged \> 18 years. Ability to provide written informed consent.
Exclusion
- Emergent surgical patients, patients with a BMI \< 35kg/m2, patients not competent to give informed consent, pregnant patients (women of child bearing potential who want to participate will have a pregnancy test done prior to enrollment in the study), patients with implantable electronic devices (pacemakers, stimulators, etc.); predictable interference with surgical procedure or standard of care.
Key Trial Info
Start Date :
February 1 2013
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
April 30 2024
Estimated Enrollment :
90 Patients enrolled
Trial Details
Trial ID
NCT01825278
Start Date
February 1 2013
End Date
April 30 2024
Last Update
May 3 2024
Active Locations (1)
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1
Tufts Medical Center
Boston, Massachusetts, United States, 02111