Improved Chest CT Diagnostic and Contrast Medium Administration
NCT ID: NCT05645796
Last Updated: 2023-03-29
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
360 participants
INTERVENTIONAL
2021-08-02
2023-01-15
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Comparison of Contrast Agent Administration Protocols
NCT04300972
Risk Factors and Computed Tomography Findings in COVID-19.
NCT04577105
On Dose Efficiency of Modern CT-scanners in Chest Scans
NCT04996693
Fully Automated Scan Technique Optimisation of Scan Timing in Chest CT
NCT03658200
Flavoring Oral Contrast for MR Enterography
NCT02617576
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
The most important patient-related factors affecting the magnitude of vascular and parenchymal contrast enhancement are body weight. Historical practice has been to use a fixed volume of CM independent of body weight. Research has shown a clear relationship between vessel enhancement and patient weight, and that fixed CM volume technique is inappropriate, as smaller patients may receive excessive volume, and larger patients insufficient volume resulting in reduced image quality and poor diagnostic. In addition, excess CM can result in contrast induced adverse effects and nephropathy. To overcome these problems, it is essential to adjust the CM volume to the patient's total body weight and body composition. This adjustment can be done in different ways. The aim of this study is to identify which weight/body tailored CM administration is the best replacement for fixed CM administration in chest CT. The cost and procedure time will also be explored.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
DIAGNOSTIC
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Fixed group
They received a fixed amount of contrast media prior to CT scan
Adopted contrast media amount by using different approaches
Using different contrast media approaches recommended by literature to explore the impact on the contrast enhancement in chest CT
body composition tailored group
They received a body tailored amount of contrast media prior to CT scan
Adopted contrast media amount by using different approaches
Using different contrast media approaches recommended by literature to explore the impact on the contrast enhancement in chest CT
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Adopted contrast media amount by using different approaches
Using different contrast media approaches recommended by literature to explore the impact on the contrast enhancement in chest CT
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* age \> 18 years
Exclusion Criteria
* cardiac failure
* pacemaker
* renal insufficiency (estimated glomerular filtration rate \<30 mL/min/1.73 m2)
* contraindications to contrast enhanced CT
* age \< 18 years
19 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Oslo University Hospital
OTHER
Oslo Metropolitan University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Safora Johansen
Associate professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Safora F Johansen, PhD
Role: STUDY_DIRECTOR
Oslo Metropolitan University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
OsloMet University
Oslo, , Norway
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Henning MK, Gunn C, Arenas-Jimenez J, Johansen S. Strategies for calculating contrast media dose for chest CT. Eur Radiol Exp. 2023 Jun 12;7(1):29. doi: 10.1186/s41747-023-00345-w.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2016/674
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.