Retrospective Evaluation of Delirium Data From Previous Study Patients for Studies at the Clinic for Anesthesiology and Intensive Care Medicine CCM/CVK/CBF
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Delirium. Basic parameters: 18 years — 100 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Germany
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
Evaluation of several studies of the Clinic for Anesthesiology and Intensive Care Medicine CCM/CVK/CBF to create a register with the delirium data from anesthesiology study patients between 18 - 100 years. The primary purpose of the register is to assess factors influencing the development of delirium. In a subproject, risk factors that may lead to the development of postoperative delirium in the elderly will be evaluated with regard to gender differences using patients from the age of 60 with different surgical procedures. The risk factors examined are based on the evidence-based and consensus-based recommendations of the ESA guideline and literature review. In addition, the delirium incidence rate and the delirium severity is examined regarding gender differences.
Primary outcome measures
- Delirium [Time frame: Up to 5 years]
Secondary outcome measures (12)
- Sedation scales [Time frame: Up to 5 years]
- Socioeconomic information 1 [Time frame: Up to 5 years]
- Socioeconomic information 2 [Time frame: Up to 5 years]
- Socioeconomic information 3 [Time frame: Up to 5 years]
- Comorbidities [Time frame: Up to 5 years]
- Charlson comorbidity index [Time frame: Up to 5 years]
- Lifestyle risks 1 [Time frame: Up to 5 years]
- Lifestyle risks 2 [Time frame: Up to 5 years]
- Lifestyle risks 3 [Time frame: Up to 5 years]
- Lifestyle risks 4 [Time frame: Up to 5 years]
- Level of education [Time frame: Up to 5 years]
- Quality of life - relatives [Time frame: Up to 5 years]
Eligibility criteria
Inclusion criteria
- Male and female patients age ≥ 18 years of studies of the clinic for Anesthesiology and Intensive Care Medicine CCM/CVK/CBF
Exclusion criteria
- None
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Germany · 1 center
- Department of Anaesthesiolgy and Intensive Care Medicine CVK/CCM, Charité - Univeristy Med — Berlin
Identifiers
NCT: NCT05913531 · Retro-Delirium