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Construction and Application of a Risk Prediction Model for Tracheal Intubation Intolerance in General Anesthesia the Recovery Period

Construction and Application of a Risk Prediction Model for Tracheal Intubation Intolerance in General Anesthesia the Recovery Period

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500110941
Enrollment
Unknown
Registered
2025-10-22
Start date
2025-10-29
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Endotracheal intubation intolerance

Interventions

Group of endotracheal tube intolerance:None
Group of no endotracheal tube intolerance:None

Sponsors

Affiliated Hospital of Jiangsu University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1 Age criteria: Age >= 18 years; 2 Anesthesia and surgery criteria: General anesthesia with endotracheal intubation and operation duration = 5; 5 Informed consent criteria: Voluntary participation with signed informed consent form.

Exclusion criteria

Exclusion criteria: 1 Dysphagia: Presence of swallowing difficulties or abnormal swallowing reflexes; 2 Mental illness or cognitive impairment: Presence of psychiatric disorders or cognitive dysfunction, rendering patients unable to accurately cooperate with the study or provide subjective feedback; 3 Severe data deficiency: Critical data missing during observation indicator collection, making effective analysis impossible; 4 Voluntary withdrawal: Patients request to exit the study during the research process; 5 Serious adverse events: Incidents such as asphyxia due to catheter intolerance or massive hemorrhage requiring immediate termination and emergency intervention; 6 Disease deterioration: Sudden postoperative worsening of the patient's condition (e.g., severe bleeding, septic shock) necessitating prioritized treatment and study termination; 7 Other unforeseen factors: Emergence of unpredictable circumstances severely disrupting study progress or endangering patient safety, leading to termination upon research team consensus.

Design outcomes

Primary

MeasureTime frame
Endotracheal tube intolerance score;incidence of endotracheal tube intolerance events;Sensitivity of the predictive model;Specificity of predictive models;

Secondary

MeasureTime frame
Awakening quality;Analgesic and sedative effects;Complications occurrence;Adverse reactions after extubation;

Countries

China

Contacts

Public ContactWang Yiting

Affiliated Hospital of Jiangsu University

1047885293@qq.com+86 157 5129 1305

Outcome results

None listed

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