Evaluation of Patient Stress Level Caused by Radiological Investigations in Early Postoperative Phase After Craniotomy
NCT ID: NCT05112575
Last Updated: 2023-12-07
Study Results
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Basic Information
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TERMINATED
152 participants
OBSERVATIONAL
2020-09-20
2023-02-01
Brief Summary
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The primary endpoint of the study is the extent of subjective distress due to postoperative MRI and CT monitoring in relation to the time interval after surgery Data will be prospectively collected from all patients aged 18 to 80 years who receive postoperative MRI or CT follow-up after craniotomy for resection of a cerebral tumor (benign and malignant) or vascular surgery.
This study determines, whether a timing of postoperative imaging can improve patient satisfaction and reduce pain, stress and discomfort caused by postoperative imaging. The outcome corresponds to the value-based medicine approach of modern patient-centred medicine. Results will be published in peer-reviewed journals and electronic patient data will be safely stored for 15 years.
Detailed Description
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Objectives The goal of this study is to assess whether early imaging with MRI (within 36 hours) after craniotomy is different regarding patient stress, than delayed imaging (between 36 and 72 hours). Secondly, the authors want to assess whether there is a difference in patient stress level between postoperative MRI and CT within 72 hours postoperatively.
The authors hypothesize that delayed imaging with MRI after craniotomy is more comfortable for patients without negative implication of radiological assessment, than imaging within 36 hours. Secondly, the authors hypothesize that postoperative MRI is more stressful for patients than CT.
Trial design The IPAST-CRANIO study (Evaluation of patient STress level caused by radiological Investigations in early Postoperative phase After CRANIOtomy) is a patient-oriented, prospective, exploratory cohort study.
Methods: Participants, interventions and outcomes Data will be collected from patients between 18 and 80 years old who receive MRI or CT follow-up after craniotomy for resection of a space occupying lesion (benign or malignant) or vascular procedure at the Department of Neurosurgery at the University Hospital Zurich
Conditions
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Keywords
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Early imaging: within 36 hours postoperatively.
Patients fulfilling eligibility criteria between 18 and 80 years old who receive MRI or CT follow-up after craniotomy for resection of a space occupying lesion (benign or malignant) or vascular within 36 hours after neurosurgical procedure.
Postoperative imaging with magnetic resonance imaging or computed tomography
Postoperative imaging control with magnetic resonance or computed tomography after craniotomy for vascular or neurooncological operations.
Late imaging: between 36 and 72 hours postoperatively
Patients fulfilling eligibility criteria between 18 and 80 years old who receive MRI or CT follow-up after craniotomy for resection of a space occupying lesion (benign or malignant) or vascular between 36 and 72 hours after neurosurgical procedure.
Postoperative imaging with magnetic resonance imaging or computed tomography
Postoperative imaging control with magnetic resonance or computed tomography after craniotomy for vascular or neurooncological operations.
Interventions
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Postoperative imaging with magnetic resonance imaging or computed tomography
Postoperative imaging control with magnetic resonance or computed tomography after craniotomy for vascular or neurooncological operations.
Eligibility Criteria
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Inclusion Criteria
* Age between 18 and 80 years
* Planned for supra- or infratentorial (partial) resection of space occupying lesion (benign or malignant) or vascular neurosurgical procedure (clipping of an aneurysm, resection of an arteriovenous malformation, resection of cavernoma)
* Patients planned for MRI or CT follow-up within 72 hours after surgery
Exclusion Criteria
* Operation using only one burr hole (e.g. biopsy)
* Not able to fill out the questionnaires due to cognitive impairment or aphasia
* Not understanding German or English language
* Contraindication for MRI examination
* No postoperative MRI or CT examination planned within 72 hours after surgery
18 Years
80 Years
ALL
No
Sponsors
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University of Zurich
OTHER
Responsible Party
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Locations
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Department of Neurosurgery, University Hospital Zurich
Zurich, , Switzerland
Countries
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References
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Tosic L, Thoma M, Voglis S, Hofer AS, Bektas D, Pangalu A, Regli L, Germans MR. Evaluation of patient STress level caused by radiological Investigations in early Postoperative phase After CRANIOtomy (IPAST-CRANIO): protocol of a Swiss prospective cohort study. BMJ Open. 2022 Sep 21;12(9):e061452. doi: 10.1136/bmjopen-2022-061452.
Other Identifiers
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2020-01590
Identifier Type: -
Identifier Source: org_study_id