Trial of Point-of-treatment Xpert MTB/RIF Assay

Tuberculosis Clinical Trial

— TBNEATXpert  

Official title:

Multicentre Randomised Control Trial of Point-of-treatment (Clinic-based) Xpert MTB/RIF Assay

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01554384
• Other study ID #: TBNEATXpertRCT
• Secondary ID: IP.09.32040.009
• Status: Completed
• Phase: N/A
• First received: July 7, 2011
• Last updated: June 4, 2013
• Start date: October 2010
• Est. completion date: July 2012

Study information

• Verified date: June 2013
• Source: University of Cape Town
• Contact: n/a
• Is FDA regulated: No
• Health authority: South Africa: Human Research Ethics Committee
• Study type: Interventional

Clinical Trial Summary

Xpert MTB/RIF assay is a novel automated molecular tool for the diagnosis of TB. Xpert can detect TB genetic material in sputum samples as well as test for genetic resistance to rifampicin providing results within 2 hours. Xpert received WHO endorsement in December 2010. There is limited data on the impact of Xpert on time-to-treatment and TB-related patient morbidity in primary care clinics. No studies have yet evaluated Xpert performed at the point-of-treatment (POT) i.e. in primary care clinic location. The investigators hypothesize that one sputum GeneXpert MTB/RIF assay performed at the POT will improve time-to-diagnosis, time-to-treatment and TB related patient morbidity for patients with suspected TB presenting to primary level TB clinics in high HIV prevalent settings.

Description:

Tuberculosis (TB) is one of the world's most important infectious causes of mortality and continues to kill 1.8 million people annually. Despite intensified standard measure of TB control, TB case detection rates are low, posing major hurdles for TB control. It is estimated that approximately 50% of patients with TB are still not diagnosed and treated appropriately. The problem is compounded by the increasing prevalence of multi drug resistant (MDR) and extensively drug resistant (XDR) TB and the close association between TB and HIV infection.

Diagnostic tools introduced 100 years ago are still in routine use and increasingly inaccurate if the face of the HIV and TB syndemics. Consequently, many patients with active TB remain undiagnosed and continue to spread the disease within the community. Thus, missed or delayed diagnosis results in ongoing transmission, patient morbidity and mortality, and social and economic consequences. Currently, there is no available point-of-care, or even point-of-treatment test that allows early detection of active tuberculosis at the peripheral health clinic level. Lack of rapid, simple and accurate diagnostic tests at this level is a major hurdle in controlling the global burden of TB. A number of promising new TB diagnostics have shown initial promise but there remains an urgent need to assess their impact when used at the point-of-treatment in primary care level.

In 2009, Cepheid released the Xpert® MTB/RIF Assay, which is the only system able to deliver answers directly from unprocessed samples by combining on-board preparation of the sample with real-time polymerase chain reaction (PCR) in less than 2 hours. Additionally, the Xpert® MTB/RIF Assay allows for simultaneous on-demand molecular testing for the detection of mycobacterium tuberculosis (M.tb) and rifampicin (frontline anti-TB drug) resistance. . The GeneXpert™ system consists of a GeneXpert instrument, personal computer and disposable fluidic cartridges. The system combines cartridge-based sample preparation with amplification and detection in a fully integrated and automated nucleic acid analysis instrument. Xpert has now been shown to be an accurate tool for the rapid diagnosis of tuberculosis in both smear-positive and smear-negative samples in both a multicentre evaluation and demonstration study with a sensitivity of approximately 70% in smear negative culture positive TB. Xpert testing in both these studies was performed at microscopy laboratories. In December 2010, on the basis of these results, Xpert was endorsed for TB diagnosis by the World Health Organisation (WHO) but is yet to be integrated into national tuberculosis control programmes.

Limited data is available on the impacts of Xpert on patient important outcomes such as TB-related morbidity. No data is available about the feasibility and robustness of performing Xpert in primary care clinics at the POT using minimally trained nursing staff. The objective of this study will be to examine the feasibility and impact of a single point-of-treatment Gene Xpert MTB/RIF Assay performed by clinic staff compared to standard microscopy-centre based diagnostics. Special focus will be on the patient-related outcomes of time-to-treatment initiation, drop out rates and the mean difference in TB-morbidity scores in patients diagnosed with Xpert.

The Xpert POT study will be a multicentre patient-level randomised controlled trial comparing a single sputum GeneXpert MTB/RIF Assay performed at point-of-treatment with same-day standard fluorescent smear microscopy for TB diagnosis at the primary level of care. A single liquid MGIT culture performed a regional laboratory will be used as the reference standard.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 1472
• Est. completion date: July 2012
• Est. primary completion date: July 2012
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Able and willing to give informed consent

2. Ambulant patient presenting to TB clinic

IF HIV negative requires 2 or more of the following:

• Cough = 2 weeks

• loss of weight

• persistent fever = 2 weeks and/or

• a single recorded temp > 38°C

• night sweats

• generalized fatigue

• hemoptysis or

• chest pain

OR if HIV positive - any one of the following:

• current cough

• night sweats

• fever

• loss of weight

3. Patient 18 years or above

Exclusion Criteria:

1. Inability to provide informed consent (e.g. mentally impaired)

2. Unable to produce 2 sputa of = 1ml

3. TB treatment within the last 60 days

4. Unable to potentially return for study follow-up at 2 and 6 months (i.e. leaving community)

5. Patient not meeting inclusion criteria

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Open Label, Primary Purpose: Diagnostic

Related Conditions & MeSH terms

• Tuberculosis

Intervention

Procedure:
• Xpert MTB/RIF assay
Automated nucleic-acid amplification test (fully integrated) test for TB
• Smear microscopy
Smear microscopy involve sputum smear with either ziehl-neelsen or auramine-O staining of slides and light or fluorescence microscopy reading

Locations

Country	Name	City	State
South Africa	University of Cape Town	Cape Town	Western Cape
South Africa	Medical Research Council	Durban	Kwazulu-Natal
Zambia	University Teaching Hospital of Zambia	Lusaka
Zimbabwe	University of Zimbabwe	Harare

Sponsors (9)

Lead Sponsor	Collaborator
University of Cape Town	Biomedical Research and Training Institute, Mbeya medical research program, McGill University, Medical Research Council, South Africa, Radboud University, University of Cape Town Lung Institute, University of Zambia, University of Zimbabwe

Countries where clinical trial is conducted

South Africa,  Zambia,  Zimbabwe, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Difference in TB-related Morbidity	Time-specific (2 month) difference in morbidity between the Xpert MTB/RIF and smear microscopy study arms.; Morbidity will be assessed using the TB Score and Karnosky performance scale	2 months	No
Primary	Difference in TB-related Morbidity	Time-specific (6 month) difference in morbidity between the Xpert MTB/RIF and smear microscopy study arms.; Morbidity will be assessed using the TB Score and Karnosky performance scale	6 months	No
Secondary	Time-to-diagnosis	Time from study enrollment to TB diagnosis in each study arm; A diagnosis of TB will include: i) Smear microscopy: WHO classification for smear grading considered positive ii) Xpert MTB/RIF positive (mtb detected) iii) MGIT liquid culture positive	6 months	No
Secondary	Drop-out and lost-to-follow up rates	Number of patients that are enrolled, randomized to a study arm, and then do not return to receive a positive test result, and Number of patients that are enrolled, randomized to a study arm, diagnosed with TB, and then are lost-to-follow up prior to completion of prescribed standard TB treatment	1 year	No
Secondary	Feasibility of clinic-based performance of Xpert MTB/RIF assay performed by nursing staff without formal research training	Feasibility indicators for the performance of Xpert at POT will be recorded. These include indeterminate rates, turn-around-time, user appraisal and assessments and performance comparisons between laboratory and clinic-based Xpert MTB/RIF.	6 months	No
Secondary	Individual patient-level cost analysis, cost-effectiveness evaluation and quality of health indices evaluation	Detailed documentation of patient and health system costs for TB diagnosis and treatment will be done at baseline, 2 month and 6 month time-points as well as quality of life health questionaires.	1 year	No
Secondary	Time-to-treatment initiation	The time-to-treatment initiation for TB culture positive patients in each study arm will be compared Treatment commencement will be considered as the initiation of the first dose of anti-TB treatment at a registered DOTs facility	6 months	No

External Links

•   Official TB NEAT consortium website