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| Name | Class |
|---|---|
| Taipei Veterans General Hospital, Taiwan | OTHER_GOV |
| National Taiwan University Hospital | OTHER |
| Chang Gung Memorial Hospital | OTHER |
| Far Eastern Memorial Hospital |
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Tuberculosis remains an important global health problem, and the world is currently not on track to end the TB epidemic by 2030. With the concerted efforts of the government and medical community, the incidence of TB in Taiwan has gradually decreased, however, Taiwan remains an endemic area for TB. The development of efficacious, safe, and shorter treatment regimens could significantly improve treatment completion rate and reduce transmission of TB. The current treatment guidelines for drug-susceptible TB from the World Health Organization (WHO), American Thoracic Society (ATS), United States Center for Diseases Control (U.S. CDC), Infectious Diseases Society of America (IDSA) and European Respiratory Society (ERS) include 2 months of isoniazid, rifampin, pyrazinamide and ethambutol (HREZ), followed by 4 months of isoniazid, rifampin, and ethambutol(HRE). The current treatment regimen requires 6 months of treatment, despite being highly efficacious, requires long duration of treatment. Adherence to treatment is the major barrier which poses a negative impact to TB control, and increased cost to both the patient and the public health system. Developing an efficacious, safe and short treatment regimen can significantly improve TB management and treatment success rates.
This prospective, multicenter, randomized, open-labeled 3-year study, will recruit 270 adult patients with newly diagnosed tuberculosis with low risk of recurrence, and randomized 1:1 to a 4 months 2HREZ/2HRE (n=135) versus standard, 6 months regimen 2HREZ/4HRE (n=135). Expected enrollment will be 90 patients in year 1, 90 in year 2 and 90 in year 3.
This study aims to evaluate the efficacy, safety and long-term recurrence rate of a short-course, 4-months regimen including 2HREZ/2HRE compared with the standard 6-months regimen, 2HREZ/4HRE, and the impact of short regimen on reducing the costs and loading to the public health and medical system
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Intervention/Treatment | Experimental | Two months of isoniazid (H), ethambutol (E), rifampicin (R) and Pyrazinamide (Z) followed by HR(E) for another two months |
|
| 6-months HERZ (2HERZ/4HRE) | Active Comparator | Two months of isoniazid (H), pyrazinamide (Z), rifampicin (R) and Pyrazinamide (Z) followed by HR(E) for another four months |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| 4-month regimen (2HERZ/2HRE) | Drug | 4-month (2HERZ/2HRE) |
| |
| Measure | Description | Time Frame |
|---|---|---|
| TB disease free survival at 12 months post-randomization | Number of participants without TB disease at 12 months after randomization | 12 months |
| TB disease free survival at 24 months post randomization | Number of participants without TB disease at 24 months after randomization | 24 months |
| Grade 3-5 adverse events | Development of Grade3-5 adverse events during treatment | From enrollment to the end of treatment at 4 or 6 months |
| Measure | Description | Time Frame |
|---|---|---|
| Early sterilizing activity | The proportion of patients with a negative sputum culture at the end of intensive phase therapy at 8 weeks | 8 weeks |
| Sputum culture conversion | Time to stable sputum culture conversion |
| Measure | Description | Time Frame |
|---|---|---|
| HLA associations with severe drug adverse events | HLA Genotyping to detect predictors for occurrence of severe drug adverse events including skin rash and hepatitis. | Upon joining or within two weeks of study entry |
Inclusion Criteria:
Newly diagnosed pulmonary tuberculosis patients combined with any of the following diagnostic conditions:
Those who have had tuberculosis in the past and have been cured for at least three years can be included
Aged over 20 years old
Laboratory data at the time of inclusion in the study or within 14 days:
Patient signs consent form
Patients who agree to join and cooperate with the county and city health bureau's urban treatment plan to ensure medication compliance.
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Susan Shin-Jung Lee, M.D., Ph.D. | Contact | +886-7342-2121 | 72029 | ssjlee28@yahoo.com.tw |
| Mei-Ling Lin, University | Contact | +886-7342-2121 | 72062 | ed101622@gmail.com |
| Name | Affiliation | Role |
|---|---|---|
| Susan Shin-Jung Lee, MD, PhD | Kaohsiung Veterans General Hospital. | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Far Eastern Memorial Hospital | Recruiting | New Taipei City | Bangiao | 220 | Taiwan |
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| OTHER |
| E-DA Hospital | OTHER |
| Kaohsiung Medical University | OTHER |
Two months of isoniazid (H), pyrazinamide (Z), rifampicin (R), and pyrazinamide (Z) Subsequent orders are for H(E)Z for another two months
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Masking will not be done
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| 6-month (2HERZ/4HRE) |
| Drug |
2 months of HREZ followed by 4 months of HR/HRE |
|
| 4, 8, 12, 16,20,24 weeks,3, 6, 12 and 24 months after treatment |
| All-cause mortality | All-cause mortality at 4 months and 12 months post-treatment assignment | 4, 12 months |
| Attributable mortality | Attributable mortality at 4 months and 12 months post-treatment assignment | 4, 12 months |
| Changes in interferon-gamma levels | Changes in interferon-gamma levels during treatment compared to baseline | 2, 4, 8, 12,16or 24 weeks |
| Changes in tumor necrosis factor-alpha levels | Changes in tumor necrosis factor-alpha levels during treatment compared to baseline | 2, 4, 8, 12,16or 24 weeks |
| Changes in interleukin-12 and interleukin-6 levels | Changes in interleukin-12 and interleukin-6 levels during treatment compared to baseline | 2, 4, 8, 12,16or 24 weeks |
| Changes in triggering receptor expressed on myeloid cells-1 (TREM-1) levels | Changes in triggering receptor expressed on myeloid cells-1 (TREM-1) levels during treatment compared to baseline | 2, 4, 8, 12,16or 24 weeks |
| Taichung Hospital | Recruiting | Taichung | West | 199 | Taiwan |
|
| E-DA Healthcare Group | Recruiting | Kaoshiung | Yanchao | 82445 | Taiwan |
|
| Kaohsiung Medical University Chung-Ho Memorial Hospital | Recruiting | Kaohsiung City | 80756 | Taiwan |
|
| Kaohsiung Veterans General Hospital | Recruiting | Kaohsiung City | 813 | Taiwan |
|
| Taipei Veterans General Hospital | Recruiting | Taipei | 112 | Taiwan |
|
| National Taiwan University Hospital | Recruiting | Taipei | Taiwan |
|
| Linkou Chang Gung Memorial Hospital | Recruiting | Taoyuan City | 333 | Taiwan |
|
| ID | Term |
|---|---|
| D014397 | Tuberculosis, Pulmonary |
| D014376 | Tuberculosis |
| ID | Term |
|---|---|
| D009164 | Mycobacterium Infections |
| D000193 | Actinomycetales Infections |
| D016908 | Gram-Positive Bacterial Infections |
| D001424 | Bacterial Infections |
| D001423 | Bacterial Infections and Mycoses |
| D007239 | Infections |
| D012141 | Respiratory Tract Infections |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
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| ID | Term |
|---|---|
| D002985 | Clinical Protocols |
| ID | Term |
|---|---|
| D013812 | Therapeutics |
| D016020 | Epidemiologic Study Characteristics |
| D017531 | Health Care Evaluation Mechanisms |
| D011787 | Quality of Health Care |
| D017530 | Health Care Quality, Access, and Evaluation |
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