Evaluation Of Switching From Twice Daily Tacrolimus To Once Daily Formulation On Cardiovascular Risk (ESTTEROD)
A One-Year, Prospective, Randomized, Controlled Study Evaluating The Efficacy Of Switching From The Twice Daily Tacrolimus Formulation To The Extended Release, Once Daily Formulation To Reduce The Framingham Cardiovascular Risk Scores.
Current standard prophylactic immunosuppression in renal transplantation includes tacrolimus, a calcineurin inhibitor, dosed twice daily. In Canada, oral tacrolimus has been available as a twice daily formulation marketed as Prograf® since 1997. It has recently become available in an extended release formulation called Advagraf®, which is dosed once daily. Advagraf® has been demonstrated to be therapeutically equivalent to Prograf® in the renal transplant maintenance population, and as a result it has been is approved as an alternative to the twice daily formulation in these patients. There is an evolving and expanding positive clinical experience with Advagraf® in kidney transplantation and it has shown to be preferred by many patients, due to the diminished dosing frequency. In clinical trials, Advagraf® has been shown to have other potential benefits over Prograf® such as less inter and intra-patient variability, improved cardiovascular profiles, and improved kidney function. Compared to Prograf®, Advagraf® also has a lower Cmin or 'trough' concentration as well as a lower Cmax or 'peak' concentration. The purpose of this study is to convert stabilized renal transplant patients currently receiving Prograf® to Advagraf®, to investigate these potential therapeutic benefits.
The Framingham Risk Score and the Reynold's Risk Score are currently recommended by the Canadian Cardiovascular Society (CCS) to predict 10-year cardiovascular risk in the general population. Surrogate markers are widely used in clinical trials to shorten follow-up durations. In this study, the investigators will use the Framingham Risk Score and Reynold's Risk Score to quantify changes in estimated cardiovascular risk. The investigators also intend to examine novel inflammatory markers to investigate cardiovascular risk.
The investigators hypothesize that the more consistent drug exposure and lower Cmax noted with Advagraf® will decrease Framingham Risk Score, Reynolds Risk score as well as markers of inflammation in kidney transplant recipients.
Panoramica dello studio
Stato
Intervento / Trattamento
Tipo di studio
Iscrizione (Effettivo)
Fase
- Fase 4
Contatti e Sedi
Luoghi di studio
-
-
Saskatchewan
-
Saskatoon, Saskatchewan, Canada, S7M0Z9
- St Paul's Hospital
-
-
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- Kidney transplant patients currently stable on the twice-daily formulation and who are followed as outpatients.
- Stability is defined as change in serum creatinine of less than 10% over the last two months
- Age 18-74 years old
- At least six months after transplantation
- Lack of rejection within the last 12 weeks
- Serum creatinine less than 300 umol/L at enrolment
- Negative urine pregnancy test for female patients of childbearing potential
- Consent to the study
- Not included in a clinical trial within the last 90 days
Exclusion Criteria:
- Patients with other types of solid organ transplants
- Patients with any form of substance abuse or psychiatric disorder.
- Patients with acute or chronic diarrhea
- Patients receiving anti-lymphocyte treatment for rejection within the last six months
- Patients on cyclosporine and or not receiving a mycophenolate derivative.
- Patients with significant liver disease defined as having an elevated bilirubin by at least two times the upper value of the normal range
- Patients who have any unstable medical condition that could interfere with the study
- Patients with chronic viral infection with HIV, Hep C and HCV.
- Presence of any acute illness requiring admission to the hospital for the last 4 weeks
- Pregnancy
- Significant cardiovascular event such as MI, stroke or TIA within the last 12 weeks or uncontrolled hypertension.
- Immunosuppressant changes within the last month.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Terapia di supporto
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione incrociata
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Comparatore attivo: Once Daily Tacrolimus
Treatment Arm - Subjects are switched from the tacrolimus twice daily (Prograf®) to the once daily formulation (Advagraf®) to maintain a trough tacrolimus level of 5-8.
|
Subjects switched from the tacrolimus twice daily (Prograf®) to the once daily formulation (Advagraf®) to maintain a trough tacrolimus level of 5-8.
Altri nomi:
|
|
Comparatore attivo: Twice Daily Tacrolimus
Control Arm - Subjects are kept on Prograf® which is the Twice Daily Tacrolimus
|
Subjects are kept on Prograf® which is the Twice Daily Tacrolimus
Altri nomi:
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Lasso di tempo |
|---|---|
|
Change in the Framingham risk scores and change in the Reynolds Risk Score.
Lasso di tempo: Visit 1, Visit 3 (12 months)
|
Visit 1, Visit 3 (12 months)
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Comparison in GFR between the two groups.
Lasso di tempo: Visit 1, Visit 3 (12 months)
|
Visit 1, Visit 3 (12 months)
|
|
|
Effect of therapy on CV biomarkers, insulin resistance and lipid profile.
Lasso di tempo: Visit 1, Visit 3 (12 months)
|
CV biomarkers will be assessed by luminex and insulin resistance and lipid profile will be assessed by the Metabolic Syndrome
|
Visit 1, Visit 3 (12 months)
|
|
To look at change in the glomerular filtration rate (GFR) over the duration of the study.
Lasso di tempo: Vist 1, Visit 3 (12 months)
|
Vist 1, Visit 3 (12 months)
|
Collaboratori e investigatori
Sponsor
Collaboratori
Investigatori
- Investigatore principale: Ahmed Shoker, MD, University of Saskatchewan
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- ESTTEROD
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
Prove cliniche su Once Daily Tacrolimus
-
University of FloridaMushroom CouncilCompletato
-
New York State Psychiatric InstituteCity University of New York, School of Public HealthRitiratoDisturbo di depersonalizzazioneStati Uniti
-
San Diego State UniversityCompletato
-
Leann BirchCompletatoPeso corporeo | Comportamento materno | Comportamento infantile
-
Semaine HealthCitruslabsCompletatoDisturbo ormonaleStati Uniti
-
Almond Board of CaliforniaKGK Science Inc.CompletatoIpercolesterolemia | HDL-CCanada
-
Galderma R&DCompletatoIrritazione della pelleStati Uniti
-
Tufts UniversityCompletatoCompromissione cognitiva lieveStati Uniti
-
Medtronic - MITGCompletato
-
Boston UniversityWelch's, Inc.Completato