Fully Automated Scan Technique: Optimisation of Scan Timing in chest CT [FAST START trial]

Fully Automated Scan Technique: Optimisation of Scan Timing in chest CT [FAST START trial] - FAST START trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON46707

Enrollment

316

Registered

2017-12-13

Start date

2018-04-05

Completion date

Unknown

Last updated

2024-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

pathologieen van de longen All lung pathologiees requiring chest CT

Interventions

NVT

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients referrered for standard chest CT Patients older than 18 and competent to give informed consent

Exclusion criteria

Exclusion criteria: Hemodynamic instability; Pregnancy; Renal insufficiency (defined as Glomerular Filtration Rate (GFR)

Design outcomes

Primary

Measure	Time frame
Attenuation above 300 HU, as stated as diagnostic.	—

Secondary

Measure	Time frame
Timing, delay, objective image quality (attenuation, image noise, SNR and CNR), subjective image quality (4-point Likert scale: 1=poor image quality; 2=sufficient image quality; 3=good image quality; 4=excellent image quality) and CO (mL/min).	—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)