Ciprofol and Remimazolam for Intraoperative Neurophysiological Monitoring During Spine Surgery
NCT07718152
Anesthesia, Intraoperative Neurophysiological Monitoring
View Trial DetailsNCT Number: NCT07535450
The goal of this observational study is to learn about current pre-anaesthesia practices in Denmark and patients' experiences of pre-anaesthesia consultations as well as what matters to patients before anaesthesia.
The questions the study aims to answer are:
What are the current pre-anaesthesia practices in Danish public hospitals. How do patients experience pre-anaesthesia consultations in Danish public hospitals.
What matters to patients before anaesthesia in Danish public hospitals.
On the day of surgery, patients answer an online survey about what matters to them when undergoing anaesthesia and whether they spoke with an anaesthesiologist or nurse anaesthetist about the anaesthesia.
Data from the medical chart are obtained to support patients responses. For patients receiving a pre-anaesthesia consultation, we will summarise the degree of person-centredness experienced by patients.
Trial opening soon.
Get Notified18 year and older
All sexes
Observational
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
-
Time frame: Baseline
Open responses to the question about what matters to the patient before anaesthesia. Will be analysed using content analysis focusing on the manifest content rather than the latent content.
Time frame: Baseline
Descriptive data on how many patients had a pre anaesthesia consultation. Response options: Yes, no, don't know.
Time frame: Baseline
Patients who had a pre-anaesthesia consultation answer four questions from the subsection "Working with patients' beliefs and values" on the Person-centred Practice Inventory - Care (PCPI-C). Each item is rated on a 5-point Likert scale ranging from strongly disagree, disagree, bneutral, agree to strongly agree. The subscale score is calculated as an average of the four items. There are no reverse scoring items. A higher score indicates that patients perceive a higher quality of person-centred care, characterized by stronger alignment with their values, shared decision-making, and authentic relationships with staff.
The "Working with patients' beliefs and values" subsection consists of the follwoing questions:
"Staff make an effort to understand what is important to me" "I feel able to say to staff what is important to me" "I feel able to give staff feedback about my experience of being cared for" "In caring for me, staff use what they know about me as a person"
Time frame: Baseline
Qualitative study with semi-structured individual telephone-interviews using a phenomenological-hermeneutic approach.
Time frame: Baseline
Categorized data where patients mark their highest level of education. Data will be presented descriptively.
Time frame: Baseline
Categorical data. Patients mark their employment status. Data will be presented descriptively.
Time frame: Baseline
Data on ASA classification will be obtained from medical journals and described as crude numbers and percentages and by group (pre-anaesthesia consultation versus no pre-anaesthesia consultation)
Time frame: Baseline
Data on pre-anaesthesia assessment practices: face-to-face, telephone based, video based, administrative (review of medical charts only), other, as well as date of assessment and done by professional group (anaesthesiologist, nurse anaesthetist, or other).
Data will be obtained from medical journals and described as crude numbers and percentages and by group (pre-anaesthesia consultation versus no pre-anaesthesia consultation)
Time frame: Baseline
Type: general, regional, epidural/spinal, sedation, local analgesia. Data will be obtained from medical journals and described as crude numbers and percentages and by group (pre-anaesthesia consultation versus no pre-anaesthesia consultation
Time frame: Baseline
Data will be obtained from medicial journals and described as crude numbers and percentages and by group (pre-anaesthesia consultation versus no pre-anaesthesia consultation)
Time frame: Baseline
Data will be obtained from medical journals and described as crude numbers and percentages and by group (pre-anaesthesia consultation versus no pre-anaesthesia consultation)
Time frame: Baseline
Data will be obtained from medical journals and described as crude numbers and percentages and by group (pre-anaesthesia consultation versus no pre-anaesthesia consultation)
Time frame: Baseline
Data will be obtained from medical journals and described as crude numbers and percentages and by group (pre-anaesthesia consultation versus no pre-anaesthesia conditions)
Time frame: Baseline
Data will be obtained from medical journals and described as crude numbers and percentages and by group (pre-anaesthesia consultation versus no pre-anaesthesia consultation)
Time frame: Baseline
A response rate will be calculated based on the total number of eligible patients and the number of responses to the questionnaire.
Contact information is provided by the study sponsor or research team.
Anne H Nielsen, Associate professor
CONTACT
Hejdi Gamst-Jensen, Associate professor
CONTACT
Gødstrup Hospital
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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