CholeraROCVNCT01811771
Oral Cholera Vaccine Delivery in Rural Bangladesh
A study testing Shanchol vaccine in people with Cholera, run by International Centre for Diarrhoeal Disease Research, Bangladesh at 1 site in Bangladesh.
Trial summary
Background: Vibrio cholerae is one of the major causes of severe diarrheal disease in Bangladesh. It is estimated that there are about 450,000 cholera cases each year in Bangladesh. Cholera is prevalent in both urban and rural settings in the country. Read more about this study
- Who is it for?
- Ages 1 year and olderHealthy volunteers can take part
- Conditions the study is for
- Cholera
- What is being tested?
- Shanchol vaccine
- Type of treatment
- Vaccines, Pill or oral medicine
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 60,000 participants
- Where
- 1 siteBangladesh
- Study dates
- Aug 2012to Aug 2015
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 1 year and older
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Who may be able to join
- Apparently healthy residents
- Aged 1 year and above
- Non Pregnant women -
Who cannot join
- Age less than 1 year
- Pregnant women -
Trial locations and contacts
1 site in 1 country.
Bangladesh1 site
International Centre for Diarrhoeal Disease Research,Bangladesh
Dhaka, Dhaka Division, 1212
About this study
Official title: Impact Evaluation of Oral Cholera Vaccination in a Rural Setting Using the National Immunization System of Bangladesh
Background:
Vibrio cholerae is one of the major causes of severe diarrheal disease in Bangladesh. It is estimated that there are about 450,000 cholera cases each year in Bangladesh. Cholera is prevalent in both urban and rural settings in the country. Policy decisions about how best a new public health tool can be incorporated into the system requires evidence. Investigators have recently carried out a feasibility study of oral cholera vaccine in urban Dhaka in Mirpur (Protocol #10061). However, whether a similar system can also be utilized in a rural area in Bangladesh needs to be studied.
Read more
The hospital disease surveillance data from International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b) reveals a substantial burden of cholera from Keraniganj upazila. Investigators propose a feasibility study of oral cholera vaccination by using the existing national immunization service delivery mechanism in Keraniganj. This study will help to provide evidence for the policy makers in introducing oral cholera vaccine in preventing cholera in high risk rural areas in Bangladesh.
Hypothesis:
That icddr,b in collaboration with the Government of Bangladesh will be able to implement an oral cholera vaccine program that;
- reaches residents of rural union of Keraniganj
- reduces the incidence of diarrhea due to Vibrio cholerae
Objectives:
- Carry out cholera vaccination in one rural union in Keraniganj.
- Evaluate the impact of vaccination in reducing cholera in the study area
Methods:
Two unions in Keraniganj will be selected; around 30,000 individuals in one union will be vaccinated and impact evaluated by comparison with another similar union. After vaccination, passive cholera surveillance at the Upazila hospital will be conducted for two years on the patients from the two unions.
Outcome measures/variables:
Cholera vaccination programme will be assessed by the number of doses administered, drop-out rates between the two rounds, the proportion of vaccine wastage, and the vaccine coverage.
Proportion of diarrheal hospitalizations that are due to V. cholerae O1 between the vaccinated and non vaccinated union will be calculated and compared to assess the impact of intervention.
Read the detailed description
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.
- Conditions
- Cholera
- Being tested
- Shanchol vaccine
- Medical subject headings
- Cholera
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Shanchol vaccineBiological
Shanchol vaccine contains whole cell inactivated heat killed and formalin killed bacteria consisting of 600 ELISA Units (EU) of lipopolysaccharide (LPS). It consists of formalin-killed V. cholerae Inaba, El Tor biotype (strain Phil 6973). It also contains 300 EU LPS of heat-killed V. cholerae Ogawa classical biotype (Cairo 50); 300 EU LPS of formalin killed V. cholerae Ogawa classical biotype (Cairo 50); 300 EU LPS of heat-killed V. cholerae Inaba, classical biotype (Cairo 48); and 600 EU LPS of formalin killed V. cholerae O139 (4260B) (9). The vaccine has no detectable cholera toxin. Vaccine is packaged as liquid formulations in 1.5-ml doses. No buffer is needed for administered.This vaccine is licensed in India and WHO prequalified.
| Study group | Role | What they receive |
|---|---|---|
| Shanchol vaccine | Active comparator | Around 30,000 individuals will be vaccinated with two doses of oral cholera vaccine at least 14 days apart.All male and non-pregnant female residents above one year age will be targeted for vaccination. Receives: Biological: Shanchol vaccine |
| Non-intervention | No intervention | No intervention will be given. Health education will be provided to the study participants. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Proportion of diarrheal hospitalizations that are due to V. cholerae O1 between the vaccinated and non vaccinated union will be calculated and compared to assess the impact of intervention
Measured: within 2 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted15 Mar 2013 (estimated)
- Study startAug 2012
- Primary completionAug 2015
- Study completionAug 2015
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for CholeraStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 60,000 participants (actual)
Sponsor and investigators
- Lead sponsor
- International Centre for Diarrhoeal Disease Research, Bangladesh
- Sponsor type
- University, hospital or other
- Collaborators
- Government of Bangladesh
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01811771
- Sponsor's protocol ID
- PR-12041
- Acronym
- ROCV
- Status last verified
- Sep 2012
- First submitted
- 13 Mar 2013
- Last updated
- 14 Oct 2015
- Results posted
- No
- Data monitoring committee
- Yes
Publications
Sur D, Lopez AL, Kanungo S, Paisley A, Manna B, Ali M, Niyogi SK, Park JK, Sarkar B, Puri MK, Kim DR, Deen JL, Holmgren J, Carbis R, Rao R, Nguyen TV, Donner A, Ganguly NK, Nair GB, Bhattacharya SK, Clemens JD. Efficacy and safety of a modified killed-whole-cell oral cholera vaccine in India: an interim analysis of a cluster-randomised, double-blind, placebo-controlled trial. Lancet. 2009 Nov 14;374(9702):1694-702. doi: 10.1016/S0140-6736(09)61297-6. Epub 2009 Oct 8.
PubMed 19819004
Study at a glance
From the registry record, last updated by the sponsor on 14 Oct 2015. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Impact Evaluation of Oral Cholera Vaccination in a Rural Setting Using the National Immunization System of Bangladesh
- ClinicalTrials.gov ID
- NCT01811771
- Acronym / sponsor ID
- ROCV / PR-12041
- Conditions
- Cholera
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 60,000 participants (actual)
- Lead sponsor
- International Centre for Diarrhoeal Disease Research, BangladeshUniversity, hospital or other
- Collaborators
- Government of Bangladesh
- Study start
- Aug 2012
- Primary completion
- Aug 2015 (actual)
- Study completion
- Aug 2015 (actual)
- First posted
- 15 Mar 2013 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Background:
Vibrio cholerae is one of the major causes of severe diarrheal disease in Bangladesh. It is estimated that there are about 450,000 cholera cases each year in Bangladesh. Cholera is prevalent in both urban and rural settings in the country. Policy decisions about how best a new public health tool can be incorporated into the system requires evidence. Investigators have recently carried out a feasibility study of oral cholera vaccine in urban Dhaka in Mirpur (Protocol #10061). However, whether a similar system can also be utilized in a rural area in Bangladesh needs to be studied.
The hospital disease surveillance data from International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b) reveals a substantial burden of cholera from Keraniganj upazila. Investigators propose a feasibility study of oral cholera vaccination by using the existing national immunization service delivery mechanism in Keraniganj. This study will help to provide evidence for the policy makers in introducing oral cholera vaccine in preventing cholera in high risk rural areas in Bangladesh.
Hypothesis:
That icddr,b in collaboration with the Government of Bangladesh will be able to implement an oral cholera vaccine program that;
- reaches residents of rural union of Keraniganj
- reduces the incidence of diarrhea due to Vibrio cholerae
Objectives:
- Carry out cholera vaccination in one rural union in Keraniganj.
- Evaluate the impact of vaccination in reducing cholera in the study area
Methods:
Two unions in Keraniganj will be selected; around 30,000 individuals in one union will be vaccinated and impact evaluated by comparison with another similar union. After vaccination, passive cholera surveillance at the Upazila hospital will be conducted for two years on the patients from the two unions.
Outcome measures/variables:
Cholera vaccination programme will be assessed by the number of doses administered, drop-out rates between the two rounds, the proportion of vaccine wastage, and the vaccine coverage.
Proportion of diarrheal hospitalizations that are due to V. cholerae O1 between the vaccinated and non vaccinated union will be calculated and compared to assess the impact of intervention.
Detailed description
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.
Study design
- Primary purpose
- Prevention
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Shanchol vaccine | Active comparator | Biological: Shanchol vaccineAround 30,000 individuals will be vaccinated with two doses of oral cholera vaccine at least 14 days apart.All male and non-pregnant female residents above one year age will be targeted for vaccination. |
| Non-intervention | No intervention | –No intervention will be given. Health education will be provided to the study participants. |
Who may qualify
- Ages
- 1 year and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (3 listed)
- Apparently healthy residents
- Aged 1 year and above
- Non Pregnant women -
Key exclusion criteria (2 listed)
- Age less than 1 year
- Pregnant women -
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Shanchol vaccineShanchol vaccine contains whole cell inactivated heat killed and formalin killed bacteria consisting of 600 ELISA Units (EU) of lipopolysaccharide (LPS). It consists of formalin-killed V. cholerae Inaba, El Tor biotype (strain Phil 6973). It also contains 300 EU LPS of heat-killed V. cholerae Ogawa classical biotype (Cairo 50); 300 EU LPS of formalin killed V. cholerae Ogawa classical biotype (Cairo 50); 300 EU LPS of heat-killed V. cholerae Inaba, classical biotype (Cairo 48); and 600 EU LPS of formalin killed V. cholerae O139 (4260B) (9). The vaccine has no detectable cholera toxin. Vaccine is packaged as liquid formulations in 1.5-ml doses. No buffer is needed for administered.This vaccine is licensed in India and WHO prequalified. | Biological | Shanchol vaccine |
Primary outcome
Proportion of diarrheal hospitalizations that are due to V. cholerae O1 between the vaccinated and non vaccinated union will be calculated and compared to assess the impact of intervention
Time frame: within 2 years
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 14 Oct 2015.
- Results publication: PubMed 19819004Sur D, Lopez AL, Kanungo S, Paisley A, Manna B, Ali M, Niyogi SK, Park JK, Sarkar B, Puri MK, Kim DR, Deen JL, Holmgren J, Carbis R, Rao R, Nguyen TV, Donner A, Ganguly NK, Nair GB, Bhattacharya SK, Clemens JD. Efficacy and safety of a modified killed-whole-cell oral cholera vaccine in India: an interim analysis of a cluster-randomised, double-blind, placebo-controlled trial. Lancet. 2009 Nov 14;374(9702):1694-702. doi: 10.1016/S0140-6736(09)61297-6. Epub 2009 Oct 8.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Shanchol vaccine in people with Cholera, run by International Centre for Diarrhoeal Disease Research, Bangladesh at 1 site in Bangladesh.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 14 Oct 2015. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Bangladesh. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Proportion of diarrheal hospitalizations that are due to V. cholerae O1 between the vaccinated and non vaccinated union will be calculated and compared to assess the impact of intervention (time frame: within 2 years). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT01811771, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Oct 2015.