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NCT06184477 Clinical Trial

The Relationship Between Prolonged Hospitalization and Surgical Experience in Pediatric Tonsillectomy Cases.

Sleep Apnea Clinical Trial

Official title:
Pediatric Tonsillectomy: Surgical Experience And Prolonged Hospitalization

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06184477
Other study ID # 15
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 1, 2023
Est. completion date February 9, 2024

Study information
Verified date May 2024
Source Pamukkale University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Guided by the expertise of a seasoned surgeon at the tertiary care hospital, the training program includes performing tonsillectomy starting from the 6th month. The clinical protocol at the hospital dictates a standard one-night hospital stay for all patients, but there is potential to extend the duration in specific cases. The study endeavors to explore the correlation between extended hospitalization, surgical proficiency, patient-specific factors, and postoperative complications in pediatric patients who underwent tonsillectomy and/or adenotonsillectomy at the clinic.

Recruitment information / eligibility
Status Completed
Enrollment 350
Est. completion date February 9, 2024
Est. primary completion date December 5, 2023
Accepts healthy volunteers No
Gender All
Age group N/A to 18 Years
Eligibility Inclusion Criteria: - Patients under 18 years of age having tonsillectomy surgery - Patients whose records are available in the hospital archive Exclusion Criteria: - Inadequate information in files

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• PEDIATRIC TONSILLECTOMY; SURGICAL EXPERIENCE AND PROLONGED HOSPITALIZATION
we aim to compare hospitalization times of pediatric patients that operated by expert surgeon or young surgeon

Locations
Country Name City State
Turkey Pamukkale University Denizli

Sponsors (1)
Lead Sponsor Collaborator
Pamukkale University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Incidence of hospitalization lasting more than 24 hours december'23- january'24
Secondary Incidence of postoperative complications incidence of bleeding, respiratory problems december'23- january'24
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