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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.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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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

Other trials in Kenya

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 groups in NCT00850915
Study groupRoleWhat they receive
1Otherin 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
2Otherno 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.

  1. incidence of TB in household contacts

    Measured: 12, 18, 24 months

Secondary outcomes (5)
  1. incidence of adverse events in household contacts

    Measured: 12, 18, 24 months

  2. incidence of TB-related symptoms in household contacts

    Measured: 12, 18, 24 months

  3. proportion of household contacts starting IPT

    Measured: 12, 18, 24 months

  4. proportion of household contacts discontinuing IPT

    Measured: 12, 18, 24 months

  5. 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.

  1. First posted25 Feb 2009 (estimated)
  2. Study startApr 2009
  3. Primary completionNov 2012
  4. Study completionNov 2012

Resources

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)
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

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.

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