Comparing two types of ultrasound for patients with viral hepatitis
Comparison Between Conventional Ultrasound and Remote Ultraportable ulTrasound for Abdominal Examination in the Context of Viral Hepatitis
This study is testing whether a new ultraportable ultrasound is better than the regular ultrasound for helping patients with viral hepatitis get accurate diagnoses and feel more comfortable during the process.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 102 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Lausanne Hospitals Academic / other |
| Locations | 1 site (Lausanne, Canton of Vaud) |
| Trial ID | NCT06571981 on ClinicalTrials.gov |
What this trial studies
This study compares the effectiveness of conventional ultrasound (CUS) and ultraportable ultrasound with teleradiology capabilities (TUP) in patients diagnosed with viral hepatitis. The primary objective is to assess the performance of both ultrasound methods based on specific imaging criteria. Additionally, the study will evaluate patient satisfaction, comfort, and the reproducibility of the ultraportable ultrasound's use. By analyzing these factors, the study aims to determine which method provides better diagnostic outcomes.
Who should consider this trial
Good fit: Ideal candidates for this study are adult patients diagnosed with viral hepatitis who are scheduled for an ultrasound examination.
Not a fit: Patients who are non-compliant or unable to follow study procedures due to psychological issues or language barriers may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance the diagnostic process for patients with viral hepatitis by identifying the more effective ultrasound method.
How similar studies have performed: Previous studies have shown promising results in the use of ultraportable ultrasound technologies, suggesting potential benefits in similar contexts.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Informed Consent signed by the subject * All adult patients with viral hepatitis for which an ultrasound is planned Exclusion Criteria: * Known or suspected non-compliance * Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc. of the participant, * Previous enrollment into the current study
Where this trial is running
Lausanne, Canton of Vaud
- Lausanne University Hospital — Lausanne, Canton of Vaud, Switzerland (Recruiting)
Study contacts
- Study coordinator: Naïk Vietti Violi, MD
- Email: naik.vietti-violi@chuv.ch
- Phone: +41795560240
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.