Last updated: November 16, 2023
Sponsor: Northwestern University
Overall Status: Completed
Phase
N/A
Condition
Sleep Disorders
Bronchiectasis
Treatment
Anti-snoring device
No anti -snoring device during their procedure.
Clinical Study ID
NCT05748626
STU00218263
Ages 18-89 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Adult patients (age 18-89 years old)
- Undergoing procedures below the umbilicus requiring anesthetic sedation without aninvasive airway
- a STOP-BANG (survey) score of 2 or greater.
Exclusion
Exclusion Criteria:
- Patients who are unable to consent
- Non-English speaking
- Those requiring general anesthesia.
Study Design
Total Participants: 25
Treatment Group(s): 2
Primary Treatment: Anti-snoring device
Phase:
Study Start date:
March 06, 2023
Estimated Completion Date:
October 24, 2023
Connect with a study center
Northwestern Memorial Hospital and Prentice Women's Hospital
Chicago, Illinois 60611
United StatesSite Not Available
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