- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT01781195
Delayed CNI-based Immunosuppression With Advagraf After MELD-based Liver Transplantation (IMUTECT)
Effect of Delayed CNI-based Immunosuppression With Advagraf on Liver Function After MELD-based Liver Transplantation
Studieoversikt
Status
Forhold
Detaljert beskrivelse
The MELD-score (model of end stage liver disease) was designed to estimate the prognosis after TIPS (transjugular intrahepatic porto-systemic shunt). Nowadays it is the key-score for patients awaiting a liver graft and consists of serum-creatinine, serum-bilirubine and the INR-ratio with values between 6-40. The MELD-based liver allocation follows the sickest patient first strategy which significantly decreased outcome after liver transplantation (LTx) in Germany. There is evidence that the immune competence of very sick patients is decreased. Monocytic HLA-DR status is a marker for the function of the immune system. A reduced monocytic HLA-DR expression is indicative for a suppressed immune system.
Blood levels of Advagraf are slowly increased during the first week until the aimed tacrolimus trough levels are reached. Since therapeutic tacrolimus trough levels are reached not before the end of the first week after transplantation this is a concept for prolonged-release immunosuppression.
We assume, that high-MELD patients (MELD >20) undergoing LTx are immunosuppressed per se. Thus prolonged-release low-dose immunosuppression with Advagraf would decrease both- infection rate (CMV-reactivation, wound infection urinary tract infections, pneumonia, etc.) and side effects of immunosuppression. The immune capacity of patients will be determined by the measurement of monocytic HLA-DR status. To ensure that graft function is not impaired due to rejection episodes, liver function will be determined with the LiMAx-test, a routine procedure in our institution. After 13-C-Methacetin is given to the patient, it is metabolized to paracetamol and 13CO2 by the enzyme CYP1A2 which is localized in hepatocytes. The 13CO2/12CO2 ratio in the exhaled air correlates with liver function.
Studietype
Registrering (Forventet)
Kontakter og plasseringer
Studiesteder
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Heidelberg, Tyskland, 69120
- Rekruttering
- University Surgical Clinic
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Ta kontakt med:
- Peter Schemmer, Prof.
- Telefonnummer: +4962215636500
- E-post: Peter.schemmer@med.uni-Heidelberg.de
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Ta kontakt med:
- Daniela Hall
- Telefonnummer: +4962215636805
- E-post: Daniela.hall@med.uni-Heidelberg.de
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Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Prøvetakingsmetode
Studiepopulasjon
Beskrivelse
Inclusion Criteria:
- age >18, <65
- first liver transplantation
- Immunosuppression with Advagraf, MMF, corticosteroid
- surgery and postoperative treatment at the department for general-, visceral- and transplantation surgery
Exclusion Criteria:
- missing informed consent
- re-transplantation
- acute infection: CMV (pp65 positive), pneumonia, urinary tract infection, wound infection, reactivation of Hepatitis B/C
Studieplan
Hvordan er studiet utformet?
Designdetaljer
Kohorter og intervensjoner
Gruppe / Kohort |
|---|
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Advagraf-based immunosuppression
50 patients after liver transplantation (25 with a MELD-score ≤20 and 25 patients with a MELD-score >20) under CNI-based immunosuppression with Advagraf
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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infection rate (CMV reactivation, wound infection, urinary tract infection, pneumonia)
Tidsramme: 1-year follow-up per patient
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clinical visit: infection rate (CMV reactivation, wound infection, urinary tract infection, pneumonia)
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1-year follow-up per patient
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Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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liver function (LiMAx)
Tidsramme: one week
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LiMAx test before liver transplantation, and on postoperative days 1, 3, 7
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one week
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HLA-DR status
Tidsramme: one week
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HLA-DR status will be measured before liver transplantation and on postoperative days 3, 5, 7.
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one week
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Samarbeidspartnere og etterforskere
Sponsor
Samarbeidspartnere
Etterforskere
- Hovedetterforsker: Peter Schemmer, Prof., University Hospital Heidelberg
Publikasjoner og nyttige lenker
Studierekorddatoer
Studer hoveddatoer
Studiestart
Primær fullføring (Forventet)
Studiet fullført (Forventet)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Anslag)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Andre studie-ID-numre
- IMUTECT2013-01
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