Actively Recruiting

Age: 18Years +
All Genders
ID06762184

Comparison of the Predictive Value of APACHE II, SOFA, SAPS II, GCS and GCS-P Scores for In-hospital Mortality in Critically Ill Patients After Craniotomy

Led by Beijing Tiantan Hospital · Updated on 2025-02-11

1600

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are reviewing adult patients admitted to three ICU wards at Beijing Tiantan Hospital from 2017 to 2020 who had undergone craniotomy and stayed in the ICU for more than 24 hours. The study aims to analyze patient information, surgery details, complications, and outcomes to evaluate the ability of different scoring systems to predict patient survival. It also plans to group patients by surgery type to assess how well these scoring systems predict outcomes for each group. The study involves collecting routine scoring data used at the hospital, such as APACHE II, SOFA, SAPS II, GCS, and GCS-P scores, and verifying their accuracy. Patients will be divided into mortality and survival groups based on their outcomes. The predictive value of each scoring system will be assessed overall and within surgical indication subgroups. Participants' medical records will be reviewed retrospectively to gather baseline and surgery-related data, complications, and outcomes. Researchers will analyze the predictive value of the scoring systems over a 3-month period. The study is observational, and no experimental treatments are given. The total participation involves data collection and analysis from past hospital records without impacting patient care.

CONDITIONS

Brief Title

Scores in Critically Ill Patients After Craniotomy

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients admitted to the ICU wards between 2017 and 2020
  • Patients underwent craniotomy
  • Patients had an ICU stay of more than 24 hours
Not Eligible

You will not qualify if you...

  • Pregnant or lactating women
  • Patients enrolled in other clinical studies

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Diagnostic Evaluation

Duration - Retrospective data collection covering ICU stay and surgery period

Baseline information, surgery-related data, complications, and routine scoring assessments are collected retrospectively for participants after craniotomy and ICU admission.

Long-term Monitoring

Duration - 3 months

Participants are observed to evaluate the predictive value of different scoring systems for in-hospital mortality and outcomes over a 3-month period.

Trial Site Locations

Total: 1 location

1

Beijing Tiantan Hospital, Capital Medical University

Beijing, Beijing, Chile, 100070

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Research Team

J

Jianfang Zhou Zhou, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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Published Research Related To This Trial

Comparison of the predictive value of APACHE II, SOFA, SAPS II, GCS and GCS-P scores for in-hospital mortality in critically ill patients after craniotomy: a retrospective cohort study in a Chinese tertiary hospital.

Jianfang Zhou, Xu-Ying Luo, Hong-Liang Li...

https://pubmed.ncbi.nlm.nih.gov/41638721