Cholera
Conditions
Keywords
Cholera, Child Health
Brief summary
This study aims to determine whether single-dose azithromycin is effective in preventing cholera in children who are at extremely high risk of infection. The study will also determine the effect of this intervention on the development of antibiotic resistant bacteria. The results will inform future strategies to prevent cholera in children, and improve overall understanding of the impact of azithromycin on antibiotic resistance.
Detailed description
Vibrio cholerae causes 3 million cases of cholera and 100,000 deaths annually. An ongoing epidemic in Yemen has caused 1.7 million cases of cholera, with 58% of cholera-related deaths occurring in children. The World Health Organization (WHO) has targeted the elimination of cholera transmission by the year 2030, but the increasing burden of cholera suggests that more effective approaches are needed to prevent the disease. Access to safe water and sanitation and the use of oral cholera vaccines (OCV) are central to the WHO-proposed approach, but children remain particularly vulnerable. Children are at the highest risk of severe disease, and current cholera vaccines are ineffective in young children. In addition, natural disasters and human conflict often delay vaccination and other large-scale interventions. Effective antibiotics reduce the volume and duration of diarrhea in cholera by over 50% and bacterial shedding by 80%. They are recommended for the treatment of moderate to severe cholera. Due to limited data, there are no standards for the use of antibiotic prophylaxis for cholera, resulting in widely varied clinical practices and the frequent use of antibiotics with unproven efficacy. For this reason, the WHO Global Task Force on Cholera Control has prioritized research in this area, suggesting that further use of prophylactic antibiotics for cholera should be stopped until prospective studies designed to measure the effectiveness of antibiotic prophylaxis and its impact on antibiotic resistance can be conducted. This study will address these two knowledge gaps. This study will determine whether a single dose of azithromycin is effective in preventing V. cholerae infection in children, and evaluate the impact of its administration on antibiotic resistance in the gut. This study focuses on children because current OCVs are ineffective in young children and because children are at the highest risk of infection and mortality from cholera. While single-dose azithromycin is a preferred treatment for cholera, it has never been studied as prophylaxis. Azithromycin has also been shown to be safe and beneficial in other recent chemoprophylaxis studies in children. This is a double-blinded cluster randomized clinical trial of single-dose azithromycin to prevent cholera in children who are household contacts of a patient with cholera in Dhaka, Bangladesh. 920 children ages 1-15 years from 400 households in Dhaka, Bangladesh, who have shared cooking facilities for the prior three days with a household member with moderate to severe V. cholerae O1 infection, can participate in this study.
Interventions
Enrolled children in the intervention arm of this study will receive a single weight-based dose of azithromycin (20 mg/kg, to a maximum dose of 1 gram) administered by a trained study nurse within 12 hours of a member of their household testing positive for cholera.
Enrolled children in the placebo arm of this study will receive a single dose of non-antibiotic placebo administered by a trained study nurse within 12 hours of a member of their household testing positive for cholera.
Sponsors
Study design
Masking description
Double-blinded
Intervention model description
Each household will be randomized to either receive a single-dose of azithromycin or receive non-antibiotic placebo. All study visits after the drug administration, which occurs during the first visit, are equal for both groups.
Eligibility
Inclusion criteria
* Shared cooking facilities for the prior three days with a household member who tested positive for cholera * Age 1 to 15 years * A parent or guardian available to provide informed consent * Intention to remain enrolled in the study for 6 months
Exclusion criteria
* Participation in any other drug, device, or vaccine trial at present or within the past 30 days * Known or suspected hypersensitivity to azithromycin or other macrolide antibiotics
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Rate of V. Cholerae Infection in Household Contacts of Cholera Index Cases | 1 week | The presence of V. cholerae O1 will be determined via the culturing of specimens collected via rectal swab sampling. Rectal swab acquisition will begin on the day of azithromycin administration and repeat on days 2, 3, 5, 6, and 7 following the intervention. |
Countries
Bangladesh
Contacts
Massachusetts General Hospital
Participant flow
Recruitment details
Participants were recruited from households of index patients with culture-confirmed cholera in Dhaka, Bangladesh. Eligible participants were household child contacts 1 to 15 years of age.
Pre-assignment details
2,475 individuals provided informed consent and were considered enrolled in the study: 1,848 index patients with cholera and 627 eligible household contacts. The index patients were enrolled to identify eligible households and child contacts but were not assigned to an intervention and not included in the assessment of trial outcomes. The Participant Flow module therefore begins with the 627 child household contacts from 402 households who were assigned by household to azithromycin or placebo.
Baseline characteristics
| Characteristic | — |
|---|---|
| Age, Categorical <=18 years | 627 Participants |
| Age, Categorical >=65 years | 0 Participants |
| Age, Categorical Between 18 and 65 years | 0 Participants |
| Participants Assigned an Intervention | 627 Participants |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants |
| Race (NIH/OMB) Asian | 313 Participants |
| Race (NIH/OMB) Black or African American | 0 Participants |
| Race (NIH/OMB) More than one race | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 0 Participants |
| Race (NIH/OMB) White | 0 Participants |
| Region of Enrollment Bangladesh | 627 Participants |
| Sex: Female, Male Female | 304 Participants |
| Sex: Female, Male Male | 168 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 0 / 314 | 0 / 313 |
| other Total, other adverse events | 0 / 314 | 0 / 313 |
| serious Total, serious adverse events | 0 / 314 | 1 / 313 |