CAP accuracy in quantification of liver steatosis to be determined using liver biopsies as reference
| Group | Value | 95% CI |
|---|---|---|
| CAP Assessment | 220 | 176 – 262 |
Last reviewed · How we verify
Controlled Attenuation Parameter (CAP) in Liver Allografts
trial testing Fibroscan 402/530 in Liver Transplant in 160 participants. Completed in 1 June 2019.
| Lead sponsor | Andres Duarte-Rojo |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 160 |
| Start date | 7 September 2016 |
| Primary completion | 1 June 2019 |
| Estimated completion | 1 June 2019 |
| Sites | 3 locations across United States |
Andres Duarte-Rojo
Adults 18 to 80, any sex, with Liver Transplant or Liver Steatosis. Patients with the condition only — healthy volunteers not accepted.
Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.
CAP accuracy in quantification of liver steatosis to be determined using liver biopsies as reference
| Group | Value | 95% CI |
|---|---|---|
| CAP Assessment | 220 | 176 – 262 |
Liver stiffness measurement
| Group | Value | 95% CI |
|---|---|---|
| CAP Assessment | 6 | 4.7 – 8.7 |
The primary aim is to determine the accuracy of CAP in the quantification of liver steatosis using liver biopsies as reference. Secondarily, investigators will correlate transient elastography (TE) and CAP results, analyze possible associations between CAP/TE and post-liver transplant (LT) clinical outcomes, and evaluate the change in CAP after LT. The study aims to include as many donors as needed to achieve at least 120 transplanted liver allografts.
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
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