Nitazoxanide Treatment for Cryptosporidiosis in AIDS Patients
Colección de datos
Enfermedades Transmisibles+10
+ Enfermedades Urogenitales
+ Infecciones Transmitidas por la Sangre
Estudio de Tratamiento
Resumen
Fecha de inicio: 1 de octubre de 1995
Fecha en la que se inscribió al primer participante.This study is about evaluating the safety and effectiveness of a drug called Nitazoxanide (NTZ) in treating Cryptosporidiosis, a severe and chronic intestinal infection common in AIDS patients. The infection significantly contributes to health issues, mortality, and healthcare costs in this population. NTZ has shown antimicrobial properties that might help combat Cryptosporidial infection, making this study potentially beneficial for improving care and addressing current challenges in managing this condition. The study enrolls patients in groups of seven, with each group receiving progressively higher doses of NTZ. The first group gets the lowest dose, and subsequent groups only start therapy once all patients in the previous group have begun. To understand how the body processes a single dose, patients receive one dose on Day 1, followed by blood sampling over the next 24 hours. After this, they start the treatment phase, taking NTZ for an additional 13 days. Blood samples are taken again on Day 14 to understand how the drug behaves in the body over time. Patients responding well to the treatment stop, while those not responding continue NTZ for another 14 days. If they still don't respond, they receive an additional month of NTZ treatment. Regular visits are scheduled for assessing clinical and parasitic response, as well as for conducting safety tests.
Protocolo
Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.Se reclutarán 28 pacientes
Número total de participantes que el ensayo clínico espera reclutar.Estudio de Tratamiento
Elegibilidad
Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.Cualquier sexo
Sexo biológico de los participantes elegibles para inscribirse.De 18 a 65 años
Rango de edades de los participantes que pueden unirse al estudio.Voluntarios sanos no permitidos
Indica si personas sanas, sin la condición que se estudia, pueden participar.Condiciones
Patología
Criterios
Inclusion Criteria Patients must have: * AIDS diagnosis according to CDC criteria. * CD4 count less than or equal to 200 cells/mm3 or CD4 count greater than or equal to 200 cells/mm3 and documented cryptosporidiosis for a minimum of 4 weeks. * Cryptosporidial diarrhea as defined by: * (1) presence of Cryptosporidium oocytes in a stool specimen within 14 days of enrollment; and (2) chronic diarrhea (i.e., an average of at least 4 bowel movements per day for a minimum of 2 weeks). * Life expectancy of at least 1 month. * Ability to tolerate food by mouth. Prior Medication: Required: * Any anti-diarrheal or anti-emetic medication for which the dosage regimen has been stable for at least 1 week prior to enrollment. * Any antiretroviral medications (e.g., zidovudine, ddI, ddC) for which the dosage regimen has been stable for at least 3 weeks prior to enrollment. Allowed: Medication for prophylaxis or maintenance therapy of opportunistic infection, stable for at least 2 weeks prior to enrollment. Exclusion Criteria Co-existing Condition: Patients with the following symptoms or conditions are excluded: Grade 4 (hematologic) or Grade 3 (for all others) toxicity. (Patients with Grade 3 toxicity for hepatic parameters may be enrolled if, in the investigator's judgment, the abnormalities are due to biliary cryptosporidiosis.) Patients with the following prior conditions are excluded: * Presence of Salmonella, Shigella, Campylobacter, Yersinia, Giardia lamblia, Entamoeba histolytica, Microsporidia, Isospora, Cyclospora, or Clostridium difficile toxin in stool (based on assessment within 14 days prior to enrollment by stool ova and parasite examination, culture, and C. difficile assay). * History of intestinal Mycobacterium avium intracellular infection or intestinal Kaposi's sarcoma. * History of Cytomegalovirus colitis, unless 28 days of therapy with ganciclovir or foscarnet completed subsequent to diagnosis. Prior Medication: Excluded: * Investigational drug therapy within 14 days of enrollment, unless available under an FDA-authorized expanded access program. * Any drug or therapy with possible anticryptosporidial activity (e.g., paromomycin, spiramycin, azithromycin, clarithromycin, hyperimmune bovine colostrum) within 14 days of enrollment.
Centros del Estudio
Estos son los hospitales, clínicas o centros de investigación donde se lleva a cabo el estudio. Puedes encontrar la ubicación más cercana a ti y su estado de reclutamiento.Este estudio tiene una ubicación
New York Hosp / Cornell Med Ctr
New York, United StatesAbrir New York Hosp / Cornell Med Ctr en Google Maps