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Development and Validation of a Risk Prediction Model for Hypoxemia in thePost-Anesthesia Care Unit after Cervical Spine Surgery

Development and Validation of a Risk Prediction Model for Hypoxemia in thePost-Anesthesia Care Unit after Cervical Spine Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500115627
Enrollment
Unknown
Registered
2025-12-29
Start date
2026-01-01
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Cervical Spine

Interventions

A derivation set (70%) and a validation set (30%):None

Sponsors

The First Affiliated Hospital of Gannan Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years, regardless of sex; 2. A confirmed diagnosis of cervical spine disease, supported by imaging findings and clinical symptoms; 3. Scheduled to undergo cervical spine surgery under general anesthesia; 4. American Society of Anesthesiologists (ASA) physical status class I to III; 5. Provision of signed informed consent by the patient or their legally authorized representative for voluntary participation in the study.

Exclusion criteria

Exclusion criteria: 1. Patients with severe preoperative respiratory insufficiency, requiring long-term home oxygen therapy or with a PaO2/FiO2 ratio <= 300; 2. Patients with concomitant psychiatric disorders, impaired consciousness, or cognitive dysfunction, precluding cooperation with postoperative assessment; 3. Patients with preexisting airway stenosis, vocal cord paralysis, or other structural airway abnormalities affecting respiratory function; 4. Patients who experience intraoperative emergencies requiring resuscitation, such as cardiac arrest, massive hemorrhage, or multiple organ dysfunction syndrome; 5. Patients who are transferred directly to the intensive care unit (ICU) postoperatively instead of the post-anesthesia care unit (PACU), precluding continuous oxygen saturation monitoring during the emergence period.

Design outcomes

Primary

MeasureTime frame
SpO2;

Countries

China

Contacts

Public ContactDai Yupei

The First Affiliated Hospital of Gannan Medical University

daiyp6@mail2.sysu.edu.cn+86 152 9777 0862

Outcome results

None listed

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