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Perioperative hemodynamic changes in patients with cervical spondylosis of different segments

Perioperative hemodynamic changes in patients with cervical spondylosis of different segments

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300078617
Enrollment
Unknown
Registered
2023-12-14
Start date
2023-12-14
Completion date
Unknown
Last updated
2023-12-19

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

Conditions

Cervical spondylosis

Interventions

Atlantoaxial group (Group A) :NA
cervical spondylosis group (Group C):NA

Sponsors

Peking University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: ASA I -III; Elective surgery; Age>18 years old; Willing to participate in research and sign an informed consent form.

Exclusion criteria

Exclusion criteria: Lesions caused by infection, tumors, or tuberculosis; Anemia (hemoglobin<9g/dL); Any known secondary hypertension; Severe cardiac disease (systolic dysfunction, preoperative left ventricular ejection fraction<45%; after pacemaker implantation, persistent arrhythmia, severe valve disease); Severe lung disease; Liver and kidney dysfunction; History of allergy to anesthetic drugs; Previous history of cervical spine surgery; Expected blood loss exceeding 800mL; Accidental admission to the ICU after surgery; Cognitive impairment or communication difficulties; The patient refused.

Design outcomes

Primary

MeasureTime frame
Area under the curve of mean arterial pressure perioperatively;

Secondary

MeasureTime frame
Intraoperative dose of norepinephrine;

Countries

China

Contacts

Public ContactXu Mao

Peking University Third Hospital

anae@163.com+86 189 1148 2830

Outcome results

None listed

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