Perioperative Factors Impacting Surgical Risk and Outcomes in Children

Status

Withdrawn

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT03436667

Enrollment

Registered

2018-02-19

Start date

2018-09-19

Completion date

2022-06-01

Last updated

2022-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Orthopedic Disorder, Surgery

Brief summary

This prospective study will measure various factors in children coming in for ambulatory surgery and attempt to create a scoring system that would be able to predict post-operative outcomes.

Interventions

DIAGNOSTIC_TESTSpirometry

Lung volumes will be measured using spirometry.

DIAGNOSTIC_TESTReaction Time

PVT-192 Psychomotor Vigilance Task Monitor is a hand-held, self-contained system used for repetitive reaction time measurement.

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

6 Years to 18 Years

Healthy volunteers

Inclusion criteria

* Pediatric patients aged 6-18 years old having ambulatory orthopedic surgery with or without planned postoperative admission. * Patients need to be cooperative to under spirometry testing and reaction time measurement. If unable to perform, we will assess why they were not able (non-cooperative, inability, etc)

Exclusion criteria

* Spinal fusion

Design outcomes

Primary

Measure	Time frame	Description
Post-anesthesia care unit (PACU) length of stay	Immediately post-op	The investigators hypothesize that spirometry performance will be associated with reduced PACU length of stay

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026