At a glance
ClinicalIndex Comparison RecordN/ACompleted· 2,400 enrolled
Drug / intervention
Not specified
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Factors Predictive of Adverse Postoperative Outcomes in Children Undergoing
Children's Hospital Medical Center, Cincinnati·observational·Posted Aug 21, 2012·Updated Jan 29, 2018
In Brief
An observational study for Tonsillectomy Postoperative Adverse Events. Completed, enrolled 2,400 participants across 1 site.
Detailed Summary
The purposes of the study are to identify 1) the patient (demographic and clinical) and health care system factors predictive of immediate and late postoperative adverse outcomes in children undergoing tonsillectomy. 2) Evaluate the preoperative use of the sleep questionnaire to identify children at risk for immediate and late postoperative adverse outcomes in children undergoing tonsillectomy.
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
201220132014201520162017201820192020202120222023202420252026
Enrollment StartMay 2012
First PostedAug 2012
Primary CompletionJun 2017
Study CompletionNov 2017
TodayJul 2026
First PostedAug 21, 2012
Enrollment StartMay 1, 2012
Primary CompletionJun 1, 2017
Study CompletionNov 1, 2017
TodayJul 2, 2026
Enrollment to primary: 5.1 yearsPosted 13.9 years ago