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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02501122
Other study ID # IRB 15-00264
Secondary ID
Status Completed
Phase N/A
First received May 20, 2015
Last updated January 30, 2017
Start date December 2015
Est. completion date January 2017

Study information

Verified date January 2017
Source Nationwide Children's Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to interrogate the Partners for Kids (PFK) and the pediatric health information (PHIS) databases in addition to our own perioperative Nationwide Children's data base to look at outcomes, resource utilization, and cost trends for adenotonsillectomy in the nationally versus locally. The investigators also want compare Nationwide Children's to other regional and national tertiary pediatric institutions.


Recruitment information / eligibility

Status Completed
Enrollment 1000000
Est. completion date January 2017
Est. primary completion date January 2017
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients who undergone an adenotonsillectomy, tonsillectomy or adenoidectomy during the past 2 years (2013-2015) who have ICD-9 codes (International Classification of Diseases) in the databases

Exclusion Criteria:

- Non-adenotonsillectomy patients

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Pediatric Health Information System (PHIS), Partners for Kids (PFK) and Nationwide Children's Hospital Perioperative Database
Utilizing these databases to assess standards for quality of care measures in adenotonsillectomy patients.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Vidya Raman

Outcome

Type Measure Description Time frame Safety issue
Primary Gather data from PHIS and contrast local databases (PFK versus Nationwide Children's) The significance is to identify outcome measures, resource utilization, and cost of adenotonsillectomy nationally as well as locally. after patient's discharge, an expected average between 6 months to 2 years
See also
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Completed NCT03378830 - Pain at Home After Tonsillectomy With or Without Adenoidectomy
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Terminated NCT04879823 - Post-operative Course of Dexamethasone to Reduce Tonsillectomy Morbidity Phase 3
Completed NCT01917097 - Bradycardia Following Intraoperative Administration of Dexmedetomidine N/A
Completed NCT00849966 - Celecoxib for Pediatric Adenotonsillectomy Phase 2
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Completed NCT05364281 - The Changes of ETT Cuff Pressures After Head and Neck Positions Placed for Adenotonsillectomy and Tonsillectomy in Children
Completed NCT03551067 - Oral Dexmedetomidine for Parental Separation in Pediatrics Undergoing Adenotonsillectomy Phase 4
Terminated NCT04791761 - Non-Opioid Pain Medications After Intracapsular Adenotonsillectomy Phase 1/Phase 2