- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT01044667
A Gastrointestinal Quality of Life Study in Lung Transplant Recipients Converted From Mycophenolate Mofetil to Myfortic
Reduced Gastrointestinal Complaints and Improved Quality of Life in Lung Transplant Recipients Converted From Mycophenolate Mofetil (MMF) to Myfortic (Enteric-coated Mycophenolate Sodium, Ec-mps)
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
Subjects administered MMF as part of their immunosuppression regimen after lung transplantation have a high incidence of GI symptoms related to the known side-effects of this drug. Previous studies have shown that GI symptoms are an important predictor of health related quality of life in other solid organ transplants (1). GI complications are common after lung transplant (2). We hypothesize that lung transplant patients converted from MMF to Myfortic will have significant reduction in severity of GI complaints. We also hypothesize that improvement in the severity of GI complaints will lead to an improved quality of life in these subjects. The study also includes data to evaluate the effect of GI complaints on health related quality of life.
Patients will complete questionnaires at each visit. Calls from the patients to the lung transplant center with GI complaints will be queried and documented on the case report form by the research nurse at each study visit. Similarly, hospital admissions for GI related complaints in the cohort will be documented. Symptom severity and health related quality of life will be assessed through the following questionnaires that have previously been validated in populations other than lung transplant (1). These questionnaires are selected specifically to capture the impact of GI complaints as related to the health related quality of life. The questionnaires that will be completed by the patient:
i.Gastrointestinal Quality of Life Index (GIQLI)
• The GIQLI is a 36-item questionnaire that assess the impact of GI distress on daily life
ii.SF-36 Health Survey • "The SF-36 Health Survey is a questionnaire that capture practical, reliable, and valid information about functional health and well-being from the patients' point of view" (4)
iii.EQ-5D Health Questionnaire
• "The EQ-5D is a standardized instrument for use as a measure of health outcome. The EQ-5D provides a simple descriptive profile and a single value for health status" (5)
Patients will complete the three questionnaires at 4 outpatient visits occurring:
- when the patient comes in to an outpatient clinic visit after initial hospital discharge after lung transplantation with complaints of GI distress (Day 1-Convert to Myfortic);
- 60 Days;
- 90 days;
- 180 days
Tipo di studio
Iscrizione (Effettivo)
Fase
- Non applicabile
Contatti e Sedi
Luoghi di studio
-
-
Tennessee
-
Nashville, Tennessee, Stati Uniti, 37232-4753
- Vanderbilt University Medical Center
-
-
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- Ability and willingness to provide written informed consent and adhere to study regimen
- Recipients who are 18-70 years of age
- Patients who have undergone either single or double lung transplant are discharged on the standard MMF (no generic MMF will be used) therapy and complain of GI symptoms, thought to be related to their immunosuppressive regimen
Exclusion Criteria:
- Patients who have GI complaints thought to be due to factors other than immunosuppressive regimen
- Patients receiving steroid treatment for acute rejection
- Women of childbearing potential who do not agree to use at least two acceptable forms of contraception prior to starting study drug, while taking study drug, and for 6 weeks after stopping study drug
- Women who have a positive serum or urine pregnancy test at visit 1 and/or continuing through the study
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Altro
- Assegnazione: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Altro: Patients taking Myfortic
Lung transplant patients converted from MMF to Myfortic as part of standard of care treatment will have GI and Quality of Life assessments done at the time of conversion to Myfortic and at 60 days, 90 days and 180 days.
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Change in Gastrointestinal Quality of Life Index (GIQLI), Baseline to 60 days:
Lasso di tempo: Change from Baseline to 60 days
|
Change in GIQLI after conversion from MMF to Myfortic
|
Change from Baseline to 60 days
|
|
Change in SF-36 Health Survey, Baseline to 60 days
Lasso di tempo: Change from Baseline to 60 days
|
Change in SF-36 Health Survey after conversion from MMF to Myfortic
|
Change from Baseline to 60 days
|
|
Change in EQ-5D Health Questionnaire, Baseline to 90 days
Lasso di tempo: Change from Baseline to 60 days
|
Change in EQ-5D Health Questionnaire after conversion from MMF to Myfortic
|
Change from Baseline to 60 days
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Gastrointestinal Quality of Life Index (GIQLI)
Lasso di tempo: Day 90 and Day 180
|
Change in GIQLI after conversion from MMF to Myfortic
|
Day 90 and Day 180
|
|
SF-36 Health Survey
Lasso di tempo: Day 90 and Day 180
|
Change in SF-36 Health Survey after conversion from MMF to Myfortic
|
Day 90 and Day 180
|
|
EQ-5D Health Questionnaire
Lasso di tempo: Day 90 and Day 180
|
Change in EQ-5D Health Questionnaire after conversion from MMF to Myfortic
|
Day 90 and Day 180
|
Collaboratori e investigatori
Sponsor
Collaboratori
Investigatori
- Investigatore principale: Eric Lambright, MD, Vanderbilt University Medcial Center
Studiare le date dei record
Studia le date principali
Inizio studio
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
Altri numeri di identificazione dello studio
- Myfortic 091423
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 .
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