Intravesical Cidofovir Instillation in HSCT Recipients With Hemorrhagic Cystitis: A Single Dose Pharmacokinetic Study
Cidofovir
+ Probenecid
Maladies génito-urinaires+5
+ Maladies de la vessie urinaire
+ Cystite
Étude thérapeutique
Résumé
Date de début de l'étude : 1 septembre 2013
Date à laquelle le premier participant a commencé l'étude.Study Drug Administration: If you are found to be eligible to take part in this study, on Day 1, you may receive some fluid for hydration by vein and then cidofovir will be put into your bladder through your foley catheter. The catheter will be clamped shut for 2 hours to keep the drug inside your bladder. After 2 hours, the catheter will be unclamped so that the drug may drain out. If you were receiving bladder irrigation (where the bladder is flushed with water) as therapy for hemorrhagic cystitis, this therapy will be restarted after your dose of cidofovir. Pharmacokinetic (PK) Testing: On Day 1, blood (about 2 teaspoons each time) will be drawn for PK testing approximately 1 hour (+/- 15 minutes) before the dose, and then again at 1 hour (+/- 15 minutes), 2 hours (+/- 15 minutes), 4 hours (+/- 1 hour), 14 hours (+/- 1 hour) and 24 hours (+/- 1 hour) after the dose. A PK sample will also be drawn on Day 14 (+- 2 days) after the dose. PK testing measures the amount of study drug in the body at different time points. Virus Testing: During this study, urine and blood will be collected and used for research to test for certain viruses, including the type of infection you had when you joined this study. Before and after the cidofovir dose on Day 1, Day 3 (+/- 1 day), Day 7 (+/- 2 days) and again on Day 14 (+/- 2 days) urine and blood (about 1 teaspoon) will be collected for virus testing. Length of Study Participation: Your active study participation will be over after the Day 30 follow-up phone call (below). If you experienced a side effect, the study staff will continue checking your medical records until the side effect becomes stable or gets better. Follow-Up: On Day 3 (+/- 1 day): You will have a physical exam. Your vital signs will be measured, and you will be asked about any symptoms you may be having. Urine will be collected for routine tests Blood (about 1 teaspoon) will be drawn for routine tests. On Day 7 (+/- 2 days): You will have a physical exam. Your vital signs will be measured, and you will be asked about any symptoms you may be having. Blood (about 1 teaspoon) will be drawn for routine tests. Urine will be collected for routine tests. On Day 14 (+/- 2 days): You will be asked about any symptoms you may be having. Blood (about 1 teaspoon) will be drawn for routine tests. Urine will be collected for routine tests. On Day 30 (+/- 2 days), you will be contacted by phone and asked about any side effects you may be having. This call will take about 10 minutes. This is an investigational study. Cidofovir given by injection is commercially available and FDA approved to treat CMV in patients with HIV. Its use in this study is investigational. Up to 6 patients will take part in this study. All will be enrolled at MD Anderson.
Protocole
Cette section fournit des détails sur le plan de l'étude, y compris la manière dont l'étude est conçue et ce qu'elle évalue.6 participants à inclure
Nombre total de participants que l'essai clinique vise à recruter.Traitement
Éligibilité
Les chercheurs recherchent des patients correspondant à une certaine description appelée critères d'éligibilité : état de santé général ou traitements antérieurs du patient.Tout sexe
Le sexe biologique des participants éligibles à s'inscrire.À partir de 18 ans
Tranche d'âge des participants éligibles à participer.Volontaires sains non autorisés
Indique si les individus en bonne santé et ne présentant pas la condition étudiée peuvent participer.Conditions
Pathologie
Critères
Plan de l'étude
Découvrez tous les traitements administrés dans cette étude, leur description détaillée et ce qu'ils impliquent.Un seul groupe d'intervention est désigné dans cette étude
Cette étude ne comporte pas de groupe placebo.
Groupes de traitement
Groupe I
ExpérimentalObjectifs de l'étude
Objectifs principaux
Centres d'étude
Ce sont les hôpitaux, cliniques ou centres de recherche où l'essai est conduit. Vous pouvez trouver le site le plus proche de vous ainsi que son statut.Cette étude comporte 1 site
University of Texas MD Anderson Cancer Center
Houston, United StatesOuvrir University of Texas MD Anderson Cancer Center dans Google Maps