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Development and validation of a delirium prediction model for patients with head and neck cancer undergoing radical tumor resection and free flap reconstruction

Development and validation of a delirium prediction model for patients with head and neck cancer undergoing radical tumor resection and free flap reconstruction

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500105934
Enrollment
Unknown
Registered
2025-07-15
Start date
2025-08-01
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

postoperative delirium

Interventions

Retrospective delirium group:None
retrospective non-delirium group:None
prospective non-delirium group:None
prospective delirium group:None

Sponsors

The Affiliated Stomatological Hospital of GuangXi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Retrospective data: (1) Patients with head and neck cancer undergoing radical tumor resection and free flap reconstruction. (2) Age >= 18 years old. (3) The patients' medical records, anesthesia records, nursing records and laboratory examination and other data are complete. 2. Prospective data: (1) Patients with head and neck cancer undergoing radical tumor resection and free flap reconstruction. (2) Age >= 18 years old, regardless of gender. (3) Signed written informed consent.

Exclusion criteria

Exclusion criteria: 1. Retrospective data: (1) Patients without malignant tumors. (2) Patients without free flaps. (3) Those with incomplete case data or obvious errors. 2. Prospective data: (1) Patients with visual, auditory or language impairments. (2) Patients with mental disorders or cognitive dysfunction (preoperative MMSE score lower than the lower limit corresponding to the patient's educational level: less than 17 points for those without formal education, less than 20 points for primary school graduates, and less than 24 points for those with secondary school or above education). (3) Those who cannot cooperate to complete the follow-up for various reasons.

Design outcomes

Primary

MeasureTime frame
postoperative delirium;

Secondary

MeasureTime frame
Laboratory examination;Preoperative indicators;General information of the patient;pain;Intraoperative indicators;Perioperative sleep disorder;

Countries

China

Contacts

Public ContactQiumiao Chen

The Affiliated Stomatological Hospital of GuangXi Medical University

754771601@qq.com+86 771 535 8857

Outcome results

None listed

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