Trials / Completed
CompletedNCT03942315
Recurrence of Hereditary Hemorrhagic Telangiectasia (HHT) After Liver Transplantation
Recurrence of Hereditary Hemorrhagic Telangiectasia (HHT) After Liver Transplantation: Clinical Implications and Physiopathological Insights.
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 14 (actual)
- Sponsor
- Hospices Civils de Lyon · Academic / Other
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
Liver transplantation (LT) has been proposed as a curative treatment in hereditary hemorrhagic telangiectasia (HHT) with severe hepatic involvement. The investigating team provides a long-term evaluation of graft status after LT for HHT with a focus on the risk of recurrence. The present study included all patients prospectively followed up after LT for HHT in the Lyon Liver Transplant Unit from 1993 to 2010 with a survival of more than 1 year.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Data collection from standard follow-up after liver transplant | All patients underwent regular follow-up every 6 to 12 months after the first year post-liver transplant (LT). Complete laboratory investigations were performed at each visit. Doppler ultrasonography was performed every 1 to 3 years after LT. Computed tomography (CT) scan and/ or magnetic resonance imaging (MRI) was performed at 1, 5, 10, 15, and 20 years after LT, or when clinically indicated. All available radiological material was reviewed. Cardiac evaluation was performed regularly in patients who received transplant for cardiac failure. |
Timeline
- Start date
- 2011-01-01
- Primary completion
- 2018-02-01
- Completion
- 2018-12-01
- First posted
- 2019-05-08
- Last updated
- 2019-05-08
Source: ClinicalTrials.gov record NCT03942315. Inclusion in this directory is not an endorsement.