TuberculosisPhase 4IPTNCT00850915
Feasibility and Effectiveness of Community Based Isoniazid Preventive Therapy in Kenya
A Phase 4 study testing community IPT in people with Tuberculosis, run by KNCV Tuberculosis Foundation at 18 sites in Kenya.
Trial summary
Isoniazid preventive therapy (IPT) is a well studied clinical intervention for primary and secondary prevention of active tuberculosis (TB) after infection with Mycobacterium tuberculosis. Read more about this study
- Who is it for?
- Ages 15 years and olderHealthy volunteers can take part
- Conditions the study is for
- Tuberculosis
- What is being tested?
- community IPT
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 1,259 participants
- Where
- 18 sitesKenya
- Study dates
- Apr 2009to Nov 2012
- Phase
- Phase 4
- 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 15 years and older
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Index cases
- New sputum smear positive pulmonary tuberculosis (PTB) patients initiating treatment for TB
- HIV infected
- Resident in the catchment area of the TB diagnostic facility
- Written informed consent
- Age equal or greater than 15 years.
Contacts
- Household contacts of a HIV infected smear positive PTB
- No plans to relocate to another area for at least the next two years
- Asymptomatic (Fit) with no cough in last 2 weeks, fever, weight loss (or failure to gain weight in children), haemoptysis or chronic diarrhea at least for the last one month.
- Written informed consent
Trial locations and contacts
18 sites in 1 country.
18 sites in 1 country
Kenya18 sites
KAPSABET District Hospital
Kapsabet-Nandi, North Rift
NYALENDA
Kisumu District, Nyanza North
Makuyu H/C
Makuyu-Muranga, Central
Kadem leprosy, Migori
Migori District, Nyanza South
Muhuru Health centre, Migori
Migori District, Nyanza South
Huruma Lions -Central district
Nairobi, Nairobi North
Kangemi HC
Nairobi, Nairobi North
Blue House, Mathare
Nairobi, Nairobi South
Jericho HC
Nairobi, Nairobi South
Kibera AMREF
Nairobi, Nairobi South
MMM, Mukuru, Embakasi
Nairobi, Nairobi South
Pumwani Majengo H/C
Nairobi, Nairobi South
Remand H/C
Nairobi, Nairobi South
Soweto Kayole, Embakasi
Nairobi, Nairobi South
Lanet
Nakuru, RVS
Nakuru West
Nakuru, RVS
Narok District Hosp
Narok, RVS
Awendo SDH
Rongo District, Nyanza South
About this study
Isoniazid preventive therapy (IPT) is a well studied clinical intervention for primary and secondary prevention of active tuberculosis (TB) after infection with Mycobacterium tuberculosis. It is widely used in industrialized countries in TB outbreak management, focusing on high risk groups such as close contacts in the family, in congregate settings, and in the workplace amongst others. Individuals infected with Human Immunodeficiency Virus (HIV) have a markedly higher risk of acquiring a TB-infection and developing consequently active TB, making HIV-infected individuals a target population for IPT. Studies of IPT in HIV infected persons in the nineties demonstrated the efficacy of IPT in the prevention of active TB in Sub -Saharan Africa and more recent studies suggest that the protective effect remains present in individuals on antiretroviral therapy.
Despite the proven efficacy of IPT this intervention has not been taken up by most HIV and TB control programmes in Africa where the burden of TB/HIV is highest. The reasons for the low uptake of IPT are many and varied but include fears of expansion of isoniazid resistance and subsequently the development of multi -drug resistant TB with widespread use of IPT. Additionally screening protocols for excluding active TB and selecting persons for IPT have not been uniformly agreed upon. There have also been concerns that programmes designed to provide IPT may shift TB control programmes from their primary responsibility of finding and treating active TB. Finally it has been unclear as to which programme, between the HIV and the TB control programme, has the primary responsibility of managing the provision of the IPT intervention.
Read more
The World Health Organization and other technical agencies engaged in global TB control have recently re-emphasized the need to scale up IPT. In this proposal we outline an operational research study to evaluate the introduction of IPT at community level and to measure its effectiveness at preventing TB. The study is based on the context of expansion of Community-Based Direct Observed Therapy Short Course (CB-DOTS), home-based care and the concept of HIV prevention with positives (PwPs), where there is a real opportunity to focus on the household as a source of HIV-associated tuberculosis.
The study is designed as a cluster randomized trial. It compares the incidence of TB in household contacts including children under 5 of identified TB/HIV co-infected patients, who received IPT through proactive community intervention and those in a control group where the community was handled in the "usual way". In the intervention group household contacts of index cases of HIV positive, smear positive PTB will be visited at home and consenting contacts will be screened for active TB using a simple questionnaire. Those found to be fit will receive isoniazid 300mg (5 mg per Kg for children) once daily for 6 months, regardless of the HIV-status. Those found not to be fit will be referred for further evaluation at the nearest TB diagnostic centre. In the control group, routine care following national guidelines will be offered. This consists of contact invitation and assessment of eligibility for IPT, especially, in children less than 5 years. Both groups will be followed up monthly through household visits. Follow up will be for a total of 24 months including the six months when IPT is provided.
A confidential HIV screening test will be provided to all consenting contacts in both intervention and control group after appropriate counseling.
The primary outcome is the incidence of TB in the intervention and control household contacts. The difference in incidence between the two groups is a measure of efficacy of the intervention. In addition the efficacy of the intervention will be estimated stratified by HIV status of household contacts if data allows. Secondary outcomes are the incidence of adverse events, the incidence of TB-related symptoms, measures on the uptake of IPT (proportion of contacts starting and discontinuing IPT, treatment adherence) and programmatic indicators, i.e. percentage of persons eligible for IPT and resources needed.
- Conditions
- Tuberculosis
- Being tested
- community IPT
- Keywords
- tuberculosis, community IPT, isoniazid adverse events, tuberculosis incidence
- Medical subject headings
- Tuberculosis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
community IPTOther
In the intervention group, the household contacts of enrolled TB/HIV co-infected patient are visited at home by community health workers. Those contacts providing informed consent and considered fit (assessed by simple questionnaire) are assumed not to have active TB and are eligible for IPT. They are offered isoniazid at 300mg (5 mg per Kg for children) once daily for 6 months, regardless of their HIV-status.
In the control group, in line with routine care, eligible index cases are requested to send their contacts to the clinic for evaluation. Contacts presenting to the clinic will be screened for TB and receive IPT, if under 5 years and when active TB is ruled out as per the current national guidelines.
All contacts (both intervention and control group) are followed up monthly to assess occurrence of symptoms suggestive of TB.
| Study group | Role | What they receive |
|---|---|---|
| 1 | Other | in this arm contacts of enrolled TB-HIV index cases were actively approached and screened for TB and offered HIV testing by CHW at their homes Receives: Other: community IPT |
| 2 | Other | no interventation was done in this group, they received the regulare care and follow up following NTP guidelines Receives: Other: community IPT |
What is being measured
The primary outcome is the main question the study is designed to answer.
incidence of TB in household contacts
Measured: 12, 18, 24 months
Secondary outcomes (5)
incidence of adverse events in household contacts
Measured: 12, 18, 24 months
incidence of TB-related symptoms in household contacts
Measured: 12, 18, 24 months
proportion of household contacts starting IPT
Measured: 12, 18, 24 months
proportion of household contacts discontinuing IPT
Measured: 12, 18, 24 months
proportion of household contacts adhering to IPT treatment
Measured: 12, 18, 24 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted25 Feb 2009 (estimated)
- Study startApr 2009
- Primary completionNov 2012
- Study completionNov 2012
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for TuberculosisStudies 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 4
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 1,259 participants (actual)
Sponsor and investigators
- Lead sponsor
- KNCV Tuberculosis Foundation
- Sponsor type
- University, hospital or other
- Collaborators
- Stichting Mondiale Tuberculose (SMT), Kenya Medical Research Institute, Division of Leprosy Tuberculosis and Lung Disease, MOPHS, Kenya, Centres for Disease Control and Prevention, Kenya., Ministry of Public Health and Sanitation, Kenya, Kenya National AIDS & STI Control Programme
- Responsible party
- Principal investigator, Eveline Klinkenberg, KNCV Tuberculosis Foundation
- Investigators
- Jeremy M Chakaya, MD, Principal investigator, Centre for Respiratory Diseases Research, Kenya Medical Research InstituteEveline Klinkenberg, PhD, Principal investigator, KNCV Tuberculosis Foundation, the Netherlands
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00850915
- Sponsor's protocol ID
- UR-01-2009-IPT-KENYA
- Acronym
- IPT
- Status last verified
- May 2013
- First submitted
- 24 Feb 2009
- Last updated
- 20 May 2013
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 20 May 2013. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Feasibility and Effectiveness of Community Based Isoniazid Preventive Therapy in Kenya
- ClinicalTrials.gov ID
- NCT00850915
- Acronym / sponsor ID
- IPT / UR-01-2009-IPT-KENYA
- Conditions
- Tuberculosis
- Keywords
- tuberculosis, community IPT, isoniazid adverse events, tuberculosis incidence
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 1,259 participants (actual)
- Lead sponsor
- KNCV Tuberculosis FoundationUniversity, hospital or other
- Collaborators
- Stichting Mondiale Tuberculose (SMT), Kenya Medical Research Institute, Division of Leprosy Tuberculosis and Lung Disease, MOPHS, Kenya, Centres for Disease Control and Prevention, Kenya., Ministry of Public Health and Sanitation, Kenya, Kenya National AIDS & STI Control Programme
- Study start
- Apr 2009
- Primary completion
- Nov 2012 (actual)
- Study completion
- Nov 2012 (actual)
- First posted
- 25 Feb 2009 (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.
Isoniazid preventive therapy (IPT) is a well studied clinical intervention for primary and secondary prevention of active tuberculosis (TB) after infection with Mycobacterium tuberculosis. It is widely used in industrialized countries in TB outbreak management, focusing on high risk groups such as close contacts in the family, in congregate settings, and in the workplace amongst others. Individuals infected with Human Immunodeficiency Virus (HIV) have a markedly higher risk of acquiring a TB-infection and developing consequently active TB, making HIV-infected individuals a target population for IPT. Studies of IPT in HIV infected persons in the nineties demonstrated the efficacy of IPT in the prevention of active TB in Sub -Saharan Africa and more recent studies suggest that the protective effect remains present in individuals on antiretroviral therapy.
Despite the proven efficacy of IPT this intervention has not been taken up by most HIV and TB control programmes in Africa where the burden of TB/HIV is highest. The reasons for the low uptake of IPT are many and varied but include fears of expansion of isoniazid resistance and subsequently the development of multi -drug resistant TB with widespread use of IPT. Additionally screening protocols for excluding active TB and selecting persons for IPT have not been uniformly agreed upon. There have also been concerns that programmes designed to provide IPT may shift TB control programmes from their primary responsibility of finding and treating active TB. Finally it has been unclear as to which programme, between the HIV and the TB control programme, has the primary responsibility of managing the provision of the IPT intervention.
The World Health Organization and other technical agencies engaged in global TB control have recently re-emphasized the need to scale up IPT. In this proposal we outline an operational research study to evaluate the introduction of IPT at community level and to measure its effectiveness at preventing TB. The study is based on the context of expansion of Community-Based Direct Observed Therapy Short Course (CB-DOTS), home-based care and the concept of HIV prevention with positives (PwPs), where there is a real opportunity to focus on the household as a source of HIV-associated tuberculosis.
The study is designed as a cluster randomized trial. It compares the incidence of TB in household contacts including children under 5 of identified TB/HIV co-infected patients, who received IPT through proactive community intervention and those in a control group where the community was handled in the "usual way". In the intervention group household contacts of index cases of HIV positive, smear positive PTB will be visited at home and consenting contacts will be screened for active TB using a simple questionnaire. Those found to be fit will receive isoniazid 300mg (5 mg per Kg for children) once daily for 6 months, regardless of the HIV-status. Those found not to be fit will be referred for further evaluation at the nearest TB diagnostic centre. In the control group, routine care following national guidelines will be offered. This consists of contact invitation and assessment of eligibility for IPT, especially, in children less than 5 years. Both groups will be followed up monthly through household visits. Follow up will be for a total of 24 months including the six months when IPT is provided.
A confidential HIV screening test will be provided to all consenting contacts in both intervention and control group after appropriate counseling.
The primary outcome is the incidence of TB in the intervention and control household contacts. The difference in incidence between the two groups is a measure of efficacy of the intervention. In addition the efficacy of the intervention will be estimated stratified by HIV status of household contacts if data allows. Secondary outcomes are the incidence of adverse events, the incidence of TB-related symptoms, measures on the uptake of IPT (proportion of contacts starting and discontinuing IPT, treatment adherence) and programmatic indicators, i.e. percentage of persons eligible for IPT and resources needed.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| 1 | Other | Other: community IPTin this arm contacts of enrolled TB-HIV index cases were actively approached and screened for TB and offered HIV testing by CHW at their homes |
| 2 | Other | Other: community IPTno interventation was done in this group, they received the regulare care and follow up following NTP guidelines |
Who may qualify
- Ages
- 15 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
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 |
|---|---|---|
| community IPTIn the intervention group, the household contacts of enrolled TB/HIV co-infected patient are visited at home by community health workers. Those contacts providing informed consent and considered fit (assessed by simple questionnaire) are assumed not to have active TB and are eligible for IPT. They are offered isoniazid at 300mg (5 mg per Kg for children) once daily for 6 months, regardless of their HIV-status. In the control group, in line with routine care, eligible index cases are requested to send their contacts to the clinic for evaluation. Contacts presenting to the clinic will be screened for TB and receive IPT, if under 5 years and when active TB is ruled out as per the current national guidelines. All contacts (both intervention and control group) are followed up monthly to assess occurrence of symptoms suggestive of TB. | Other | 1, 2 |
Primary outcome
incidence of TB in household contacts
Time frame: 12, 18, 24 months
5 secondary outcomes
incidence of adverse events in household contacts
Time frame: 12, 18, 24 months
incidence of TB-related symptoms in household contacts
Time frame: 12, 18, 24 months
proportion of household contacts starting IPT
Time frame: 12, 18, 24 months
proportion of household contacts discontinuing IPT
Time frame: 12, 18, 24 months
proportion of household contacts adhering to IPT treatment
Time frame: 12, 18, 24 months
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 20 May 2013.
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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.
Jeremy M Chakaya, MD principal investigator
Centre for Respiratory Diseases Research, Kenya Medical Research Institute
Eveline Klinkenberg, PhD principal investigator
KNCV Tuberculosis Foundation, the Netherlands
18 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 4 study testing community IPT in people with Tuberculosis, run by KNCV Tuberculosis Foundation at 18 sites in Kenya.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
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 20 May 2013. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 18 sites in Kenya. 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.
What does this phase mean?
Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
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?
incidence of TB in household contacts (time frame: 12, 18, 24 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 20 May 2013.