ROCVImpact Evaluation of Oral Cholera Vaccination in a Rural Setting Using the National Immunization System of Bangladesh
Shanchol vaccine
Infecciones Bacterianas y Micosis+2
+ Infecciones bacterianas
+ Infecciones
Estudio de Prevención
Resumen
Fecha de inicio: 1 de agosto de 2012
Fecha en la que se inscribió al primer participante.This study in two selected rural cholera endemic unions in Keraniganj Upazila near Dhaka city will continue for two and half years. The study has two major components- 1. Feasibility of intervention with oral cholera vaccine in one union; and, 2. Impact evaluation of the intervention through prospective passive surveillance for diarrheal patients coming from the two selected unions at the upazila health complex. For the cholera vaccination all male and non-pregnant female residents above one year age will be targeted for vaccination in the selected union. Investigators are excluding less than one year children and pregnant woman form vaccination. For the surveillance part a standardized questionnaire will be administered to all consented diarrheal patients or their guardians in order to obtain information on diarrhea, health and demographic issues. Stool samples will be co llected and tested for V. cholerae O1 and O139. Investigators, purposively, have selected Keraniganj Upazila of Dhaka as the study area due to high incidence of diarrhea and evidence of culture confirmed cholera and its close proximity to Dhaka. Based on the Keraniganj diarrheal disease report and evidence of cholera prevalence in icddr,b surveillance data, the Ruhitpur union with approximately thirty thousand population will be selected as our area for vaccination, the intervention union. To evaluate the effectiveness of intervention Investigators will include Basta union of Keraniganj as the non-intervention area. In selecting the two unions, to make them comparable, in addition to population size, evidence of diarrhea and cholera, Investigators have considered the closeness to the Upazila Health Complexes (UHC), presence of educational institutes and health facilities, literacy rates, land area, etc. Investigators will use the killed whole cell oral cholera vaccine, "Shanchol", manufactured by Shantha Biotechnics for the study. The vaccine is registered in India and is prequalified by WHO. In urban Mirpur area investigators have already successfully used more than 265,000 doses of the same vaccine. Vaccines are stored in the EPI(Expanded program on immunization) cold room at 2-8 degree C. Based on available space in District and upazila cold stores, vaccines will be shifted from the EPI cold room facilities in Dhaka. Investigators will use the rural health facilities including community clinics as the vaccination site for vaccinating the catchment eligible targeted population. Investigators will use the existing EPI cold chain facilities at the Keraniganj Upazila health complex to deliver the vaccine in the selected union. During vaccination, vaccinators will gently shake the single dose vial well to disperse the suspension and then open it to feed its content to the recipient. Adults and older children can take the vaccine by themselves but vaccinators will feed the vaccine contents to younger children. Trained Community health care provider, Health Assistants and Family Welfare assistants of the community clinic area will act as vaccinators. There will be adequate training for all concerned prior to the vaccination programme. In addition, volunteers from the community will be recruited and trained to assist with the vaccination and social mobilization activities. Investigators will develop appropriate communication materials to inform the population about the cholera vaccination opportunity. Local health facilities, pharmacies and community residents will be involved to assist social mobilization of the population to attend vaccination sessions. Persons below one year of age and pregnant women will not receive the vaccine. People living in the adjacent unions will not be eligible to receive the vaccine, due to limited number of vaccines in hand. Investigators will have to clarify in a convincing way through the field workers, community volunteers/leaders and to the stakeholders that everyone cannot be given the intervention because of the targeted approach and unavailability of vaccine for all and because this study is only a feasibility study to test the vaccine delivery mechanism in a rural setting. All patients from the study area to the Keraniganj Upazila Health Complex (UHC) with diarrhoea will be included in cholera surveillance. All study participants will be encouraged to attend Upazila health complex for the treatment of diarrhoeal diseases at the initiation of the study and time to time will be reminded by the field workers. A patient who has in the last 24 hours three or more loose or liquid stool is defined as a case of diarrhea (13). The surveillance for cholera at the Upazila health complex will be carried out for two years. As the study is implementing passive surveillance in both the unions- intervention and control, to see the effectiveness of the intervention, the key element is to capture most of the cases coming from the two unions. To do so, the study will convey the messages to the people of the two unions to utilize the existing GoB(Government of Bangladesh) facility in the upazila health complex for diarrheal illness. Study will provide a card to the peoples in two unions which will contain such messages, while distributing the cards field workers will convey the messages and tell them to bring the cards for diarrheal illness at the Keraniganj UHC. The existing field health workers, workers in the health facilities (community clinics, health & family welfare center) will be encouraged to convey such messages and refer the diarrheal patients to the Keraniganj upazila health complex. The patients in the OPD(out patient department) and ORT(oral rehydration therapy) corners at the Keraniganj UHC will be included in the passive surveillance and other private clinics/hospital(if available and agrees) will also be taken under surveillance. Investigators will collect stool or rectal swab specimens from diarrheal patients coming from the study population for diarrheal diseases. Specimens will be evaluated for V. cholerae O1and O139 according to WHO/CDC guidelines at the icddr,b.
Protocolo
Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.Se reclutarán 60.000 pacientes
Número total de participantes que el ensayo clínico espera reclutar.Estudio de Prevención
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.A partir de 1 años
Rango de edades de los participantes que pueden unirse al estudio.Voluntarios sanos permitidos
Indica si personas sanas, sin la condición que se estudia, pueden participar.Condiciones
Patología
Criterios
Plan de Estudio
Conoce todos los tratamientos administrados en este estudio, su descripción detallada y en qué consisten.2 grupos de intervención están designados en este estudio
0% de probabilidad de ser asignado al grupo placebo
Grupos de Tratamiento
Grupo I
Comparador ActivoGrupo II
Sin IntervenciónObjetivos del Estudio
Objetivos Primarios
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
International Centre for Diarrhoeal Disease Research,Bangladesh
Dhaka, BangladeshAbrir International Centre for Diarrhoeal Disease Research,Bangladesh en Google Maps