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Can Postoperative Outcomes be Predicted From Asking OSA Screening Questions Pre-operatively?

Nationwide Children's Hospital logo

Nationwide Children's Hospital

Status

Withdrawn

Conditions

Obstructive Sleep Apnea

Treatments

Other: Survey

Study type

Observational

Funder types

Other

Identifiers

NCT02930538
IRB16-00491

Details and patient eligibility

About

The proposed research will determine whether a 6-item screening questionnaire previously shown to correlate with moderate or severe OSA is useful for predicting postoperative outcomes in children undergoing surgery under general anesthesia.

Full description

The survey will be administered preoperatively in the ENT clinic or the preoperative surgical unit. The following data will also be recorded: patient demographics (age, gender, BMI), surgical procedure, length of procedure and anesthetic, and smoking exposure. Based on differences in postoperative outcomes (e.g., supplemental oxygen requirement in the PACU) observed in the derivation cohort for the 6-item questionnaire, the study will enroll 1,000 patients to attain sufficient power for evaluating the 6-item questionnaire in the overall cohort and in demographically or clinically defined subgroups.

Sex

All

Ages

3 to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • The study will include all who are presenting for surgery to the main operating room, ambulatory surgical center or procedure center at Nationwide Children's Hospital.

Exclusion criteria

  • Emergency surgery and any caregiver or patient refusal.

Trial design

0 participants in 1 patient group

Children undergoing surgery
Description:
Children ages 3-18 undergoing a surgical procedure at Nationwide Children's Hosp.
Treatment:
Other: Survey

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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