Phase
Condition
Respiratory Syncytial Virus (Rsv) Infection
Treatment
N/AClinical Study ID
Ages < 7 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
All study participants must be undergoing general anesthesia and surgery with anendotracheal tube
The URI group will be participants with a score of at least 3 on our pre-operativeURI survey, with planned airway instrumentation with an endotracheal tube (ETT) fortheir surgical procedure who are to be discharged same day or on postoperative day
- The non URI group will be participants undergoing elective procedures with no URIsymptom or recent URI. Defined as no URI or "allergy" symptom within the past 6weeks and a score of 1 or less on the URI survey, with planned airwayinstrumentation with an ETT for their surgical procedure who are to be dischargedsame day or on postoperative day 1.
Exclusion
Exclusion Criteria:
History of home oxygen use or ventilator dependence,
Patients undergoing emergent procedures.
Patients with cyanotic congenital heart disease.
Patients receiving a surgical procedure where the duration of post procedure
admission is anticipated to be greater or equal to 2 postoperative days.
Patients undergoing anesthesia for imaging procedures alone.
Patients who are extubated deep intentionally.
Patients intended to be managed with supraglottic airway.
Patients undergoing total IV anaesthesia (TIVA).
Study Design
Study Description
Connect with a study center
Wake Forest University Health Sciences
Winston-Salem, North Carolina 27157
United StatesActive - Recruiting
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