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The Impact of Preoperative Sleep Quality on Anesthesia in Pediatric Patients with Adenoid and Tonsillar Hypertrophy

The Impact of Preoperative Sleep Quality on Anesthesia in Pediatric Patients with Adenoid and Tonsillar Hypertrophy

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500108705
Enrollment
Unknown
Registered
2025-09-03
Start date
2025-09-04
Completion date
Unknown
Last updated
2025-09-08

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

Conditions

Sleep Quality and Anesthesia

Interventions

Mild sleep apnea-hypopnea syndrome group:None
Severe sleep apnea-hypopnea syndrome:None

Sponsors

Children's Hospital of Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1. Age: 5 to 12 years old, no gender restrictions; 2. ASA anesthesia classification I to II; 3. Elective tonsillectomy and adenoidectomy; 4. Preoperative sleep apnea screening; 5. Estimated anesthesia and surgery duration <=120 minutes; 6. Informed consent signed by the child's parent or legal guardian.

Exclusion criteria

Exclusion criteria: 1. Body mass index (BMI): BMI >=28kg/m^2 or upper limit of normal reference value); hepatic impairment (ALT and/or AST > 1.5 times upper limit of normal reference value); 8. Children with a history of severe head trauma or intracranial hypertension within 6 months; 9. History of preterm labor or intrauterine growth retardation; 10. Children with chronic neurological or psychiatric disorders (e.g., autism, Tourette's syndrome, epilepsy, etc.) or inability to express their wishes correctly; 11. Children with a history of chronic sedative-analgesic medications or monoamine oxidase inhibitors; 12. Children with an expected blood loss of more than 100 ml during surgery; 13. Children with other conditions that, in the opinion of the investigator, make them unsuitable for enrollment, such as coagulation abnormalities or genetic abnormalities.

Design outcomes

Primary

MeasureTime frame
Bispectral index;Anesthetic dosage;

Secondary

MeasureTime frame
Sleep quality;Blood pressure;Heart rate;Extubation time;Duration of surgery;Awakening Time;Sleep habits;Level of anxiety;Agitation-Sedation Scale;Pain Score;Pulse Oxygen Saturation;

Countries

China

Contacts

Public ContactLiu Tingting

Children's Hospital of Zhejiang University School of Medicin

897673178@qq.com+86 158 6846 9625

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026