Correlation Analysis of POD and pNCD in Elderly Spinal Surgery Patients

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age65-100
SponsorXuanwu Hospital, Beijing

About this trial

This study is a prospective cohort study to investigate the differences in serum indexes between elderly spinal surgery patients with postoperative delirium (POD) who either develop or do not develop long-term postoperative neurocognitive disorders (pNCD).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients ≥65 years of age who have undergone spinal surgery anesthesia; Sign informed consent

Disqualifiers

Inability to complete cognitive function assessment; Illiteracy, hearing impairment or visual impairment; He has a history of epilepsy, depression, schizophrenia, Alzheimer's disease and other psychiatric and neurological diseases

Trial population

Patients 65\~100 years of age who have undergone spinal surgical anesthesia

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • no intervention

    Other intervention

    this is an observation study,no intervention

Treatment groups

165 Participants
are divided into 1 treatment group
Group A: postoperative delirium(POD) and postoperative neurocognitive disorder(pNCD)1 intervention

Trial outcomes

Primary outcomes

1

change in serum indexes between elderly spinal patients with postoperative delirium(POD) who either develop or do not develop postoperative neurocognitive disorders (pNCD) one month after surgery

Perioperative neurocognitive disorders (PND) represent one of the common complications of general anesthesia, posing serious hazards and currently being a hot topic and a challenging problem in international research. Recently, general anesthesia has led to a new breakthrough in the study of PND serum-related markers, such as brain-derived nutritional factors(BDNF)、C-reactive protein(CRP)、homocysteine(Hcy). This provides new perspectives for PND prevention, evaluation and furnishes theoretical grounds for enhancing the safety of clinical anesthesia and the quality of life for patients.

Time frame
2024.5.9-2026.5.1

Secondary outcomes

Other outcomes

Sponsors and contacts

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