Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
150 participants
OBSERVATIONAL
2025-08-30
2025-11-30
Brief Summary
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Group 1:Pediatric patients who underwent adenotonsillectomy Group 2: Pediatric patients who underwent any surgical operation We will evaluate two patient groups.
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Detailed Description
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Group 1:Pediatric patients who underwent adenotonsillectomy Group 2: Pediatric patients who underwent any surgical operation
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Group 1: Pediatric patients who underwent adenotonsillectomy
No interventions assigned to this group
Group 2: Pediatric patients who underwent any surgical operation
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
2. Pediatric patients aged 3-8
3. Those planned for elective surgery
Exclusion Criteria
2. ASA 3-4-5 patients
3. Those who will undergo emergency surgery
4. Those who will be subjected to an airway or anesthesia technique other than orotracheal intubation
5. Newborn group patients
6. Patients younger than 3 years old and older than 8 years old
3 Years
8 Years
ALL
No
Sponsors
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Izmir City Hospital
OTHER_GOV
Responsible Party
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Tuba Kuvvet Yoldaş
MD, Anesthesia Specialist
Principal Investigators
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Tuba Kuvvet Yoldas, MD, Anesthesiology Specialist
Role: PRINCIPAL_INVESTIGATOR
Izmir City Hospital
Locations
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İzmir City Hospital
Izmir, Bayraklı, Turkey (Türkiye)
Countries
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Central Contacts
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Facility Contacts
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Role: primary
Other Identifiers
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İSH-ANS-TK-02
Identifier Type: -
Identifier Source: org_study_id
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