- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT07752654
TransThoracic Ultrasound for Descending Aortic Aneurysms (THORUS)
Feasibility, Accuracy and Reproducibility of Ultrasound in Aneurysms of the Descending Thoracic Aorta
The goal of this observational study is to assess the applicability of non-invasive ultrasound in aneurysms of the descending thoracic aorta.
The main question it aims to answer is:
What is the feasibility of Ultrasound to visualise the Descending Thoracic Aorta, and can this imaging modality accurately measure the maximum size of aneurysms and residual sacs with acceptable reproducibility?
Participants are having their diagnosis confirmed or excluded by conventional imaging techniques (CT scans). Participants receive exactly the same standard of care regardless of their participation. The study offers an additional ultrasound scan, and the results will be compared with previous imaging.
Przegląd badań
Status
Szczegółowy opis
Aneurysms of the aortic artery are a significant public health issue. The number of newly diagnosed aneurysms of the thoracic aorta is on the rise, and aneurysm rupture is a catastrophic event associated with high mortality rates. The most proximal sections of the aorta (ascending and the aortic arch) are routinely scanned by echocardiography practitioners. The abdominal aorta is also easily visualised on transabdominal ultrasound, and there is a screening programme in the UK that is highly cost-effective and reduced the aneurysm-related number of deaths. However, the portion of the aorta in the chest (descending thoracic aorta) is not routinely assessed by ultrasound practitioners.
The diagnosis of descending thoracic aneurysms relies mostly on imaging techniques that use ionising radiation. In addition, these techniques are expensive and may not be widely available in some regions. In contrast, ultrasound is a non-invasive technique that allows visualisation of most parts of the body. Ultrasound machine suppliers have invested in better systems and transducers over the years and visualisation of the descending thoracic aorta may now be possible.
The main aims of this study are to assess the feasibility (Part 1), accuracy (Part 2) and reproducibility (Part 3) ultrasound in the diagnosis and monitoring of descending thoracic aortic aneurysms. Participants will be recruited from the vascular lab and outpatient clinics, and diameters of the descending thoracic aorta will be measured with non-invasive ultrasound. Data obtained from study measurements will be compared with computed tomography scans that patients had as part of their standard of care.
If the feasibility, accuracy and reproducibility of Ultrasound are clearly demonstrated, routine ultrasound scans of the descending thoracic aorta may be suggested.
Typ studiów
Zapisy (Szacowany)
Kontakty i lokalizacje
Kontakt w sprawie studiów
- Nazwa: Carlos Pinho, PhD Student
- Numer telefonu: +44 20 3312 3374
- E-mail: cv1026@ic.ac.uk
Kopia zapasowa kontaktu do badania
- Nazwa: Cheuk Fund Wong
- Numer telefonu: +44 20 7594 9832
- E-mail: rgit@imperial.ac.uk
Lokalizacje studiów
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London
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London, London, Zjednoczone Królestwo, W2 1NY
- Imperial College Healthcare NHS Trust - St Mary's Hospital
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Kontakt:
- Carlos Pinho, PhD Student
- Numer telefonu: +44 20 3312 3374
- E-mail: cv1026@ic.ac.uk
-
Kontakt:
- Cheuk Fund Wong
- Numer telefonu: +44 20 7594 9832
- E-mail: rgit@imperial.ac.uk
-
Główny śledczy:
- Carlos Pinho, PhD Student
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Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
- Dorosły
- Starszy dorosły
Akceptuje zdrowych ochotników
Metoda próbkowania
Badana populacja
Opis
Inclusion Criteria:
- Patients with diagnosed AAA or other vascular condition attending the vascular scanning department for routine ultrasound and confirmed healthy DTA (Control group).
- Patients with known DTAA (including Type B dissection) or patients who had TEVAR previously (Case group).
- Patients who have had CT as part of their standard of care.
- Patients able to tolerate the scan (Lying in supine position).
- Adults aged 18 or over.
- Willing to provide consent.
Exclusion Criteria:
- Patient under 18 years of age.
- Previous thoracic surgery or body deformity (severe kyphosis, scoliosis, pleural effusion or chest wall trauma).
- Patients without previous imaging of the thoracic aorta.
- Life expectancy <2 years.
- Pregnant Women.
- Patients unwilling to provide consent or unable to comply with study requirements.
- Patients too frail to travel to routine outpatient appointments.
- Inability to attend the appointment due to time constraints or other commitments.
- Although rare, ultrasound contraindications as described in the scanning protocol are also exclusion criteria.
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
Kohorty i interwencje
Grupa / Kohorta |
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CONTROLS
Patients with healthy DTA (30 patients)
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CASES
Patients with DTAA or TEVAR (30 patients)
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Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Part 1 - Feasibility - Proportion of participants with successful ultrasound measurement of the diameter of the descending thoracic aorta
Ramy czasowe: Day 1 - At the single ultrasound study visit.
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Number and percentage of participants in whom the descending thoracic aortic diameter can be obtained by transthoracic ultrasound.
The units of Measure are total number and percentages.
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Day 1 - At the single ultrasound study visit.
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Part 1 - Feasibility - Length of the descending thoracic aorta by Ultrasound
Ramy czasowe: Day 1 - At the single ultrasound study visit.
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Total length of the descending thoracic aorta from the aortic isthmus to the coeliac axis.
The unit of Measure is Centimetres (cms).
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Day 1 - At the single ultrasound study visit.
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Part 1 - Feasibility - Ultrasound Quality Score
Ramy czasowe: Day 1 - At the single ultrasound study visit.
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Number of ultrasound windows that allow visualisation of the descending thoracic aorta (0 to 3 windows) and allocation of a quality score. The Unit of Measure is a score created for this study (0-Windows: No views; 1 window: Poor; 2 windows: Moderate; 3 windows: Good). Higher scores mean better image quality. |
Day 1 - At the single ultrasound study visit.
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Part 2 - Accuracy - Comparision between Transthoracic Ultrasound and CT
Ramy czasowe: Day 1 - At the single ultrasound study visit.
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Calculate mean differences and limits of agreement between TUS and CT.
Achieve high sensitivity and specificity.
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Day 1 - At the single ultrasound study visit.
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Part 3 - Reproducibility - Intraclass correlation coefficient
Ramy czasowe: Day 1 - At the single ultrasound study visit.
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Calculate inter- and intra-operator variability by intraclass correlation coefficient (ICC).
The study aims to achieve good or excellent reliability.
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Day 1 - At the single ultrasound study visit.
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Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Part 1 - Feasibility - Factors limiting visualisation of the Descending Thoracic Aorta
Ramy czasowe: Day 1 - At the single ultrasound study visit.
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Number and percentages of participants in whom limiting factors such as body habitus or rib shadowing are reported after the ultrasound test.
The units of measure are the number of participants with raised BMI (kg/m^2) and acoustic shadowing due to bone density.
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Day 1 - At the single ultrasound study visit.
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Part 1 - Feasibility - Duration of Ultrasound Examination
Ramy czasowe: Day 1 - At the single ultrasound study visit.
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Total time needed to complete the ultrasound scan of the descending thoracic aorta.
The unit of measure is minutes.
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Day 1 - At the single ultrasound study visit.
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Part 1 - Feasibility - Patient Feedback Questionnaire
Ramy czasowe: Day 1 - At the single ultrasound study visit.
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Scores are obtained from the patient feedback questionnaire that was created specifically for this study and consists of 5 questions relating to comfort, tolerability and overall experience of the ultrasound scan.
The unit of measure is a score ranging from 1-Strongly Disagree to 5-Strongly Agree.
Higher scores mean better patient satisfaction.
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Day 1 - At the single ultrasound study visit.
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Współpracownicy i badacze
Sponsor
Śledczy
- Krzesło do nauki: Professor Colin Bicknell, Imperial College London
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Szacowany)
Zakończenie podstawowe (Szacowany)
Ukończenie studiów (Szacowany)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Inne numery identyfikacyjne badania
- 199470
- IRAS Project ID: 365629 (Inny identyfikator: NHS Health Research Authority)
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
Opis planu IPD
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
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