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Research on New Regimens for Retreatment Pulmonary Tuberculosis

Primary Purpose

Reinfection Pulmonary Tuberculosis

Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Isoniazid Aminosalicylate Tablets
Streptomycin injectable
Sponsored by
Shanghai Pulmonary Hospital, Shanghai, China
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Reinfection Pulmonary Tuberculosis

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Sputum confirmed diagnosis of retreatment pulmonary tuberculosis
  • Must be able to swallow tablets
  • Must be able to sign written informed consent form

Exclusion Criteria:

  • Extra-pulmonary tuberculosis
  • Diabetes
  • Allergy to any of the medications in the regimen or pregnancy
  • Liver disease
  • Renal disease
  • Metabolic disease
  • Immune system disease
  • Hematological disease
  • Nervous system and mental disease
  • Endocrine disease
  • Malignant disease
  • Receiving immunosuppressive therapy
  • HIV/AIDS
  • Alcohol addiction

Sites / Locations

  • Shanghai Pulmonary HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

arm A: super-short retreatment regimen

arm B:standardized retreatment regimen

Arm Description

A regimen of 5 drugs is to be administered. Isoniazid Aminosalicylate Tablets,0.3g tid po for 5 mon moxifloxacin tab, 0.4g qd po for 5 mon rifabutin capsule,0.3g qd po for 5 mon ethambutol tab, 0.75g qd po for 5 mon pyrazinamide tab, 0.5g tid po for 5 mon

8-9 months of standardized regimen is to be administered. regimen 1.2SHREZ/6HRE streptomycin injectable,0.75g qd intramuscular for 2 mon isoniazid tab,0.3g qd po for 8 mon rifampicin capsule,0.45-0.6g po for 8 mon ethambutol tab, 0.75g qd po for 8 mon pyrazinamide tab, 0.5g tid po for 2 mon or regimen 2.3HREZ/6HRE isoniazid tab,0.3g qd po for 9 mon rifampicin capsule,0.45-0.6g po for 9 mon ethambutol tab, 0.75g qd po for 9 mon pyrazinamide tab, 0.5g tid po for 3 mon

Outcomes

Primary Outcome Measures

success rate

Secondary Outcome Measures

adverse reaction rate

Full Information

First Posted
December 31, 2014
Last Updated
January 2, 2015
Sponsor
Shanghai Pulmonary Hospital, Shanghai, China
Collaborators
Shanghai Center for Disease Control and Prevention, Jiangsu Province Centers for Disease Control and Prevention, Zhejiang University, Centers for Disease Control and Prevention
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1. Study Identification

Unique Protocol Identification Number
NCT02331823
Brief Title
Research on New Regimens for Retreatment Pulmonary Tuberculosis
Official Title
New Super-short Course Regimen for Retreatment Pulmonary Tuberculosis
Study Type
Interventional

2. Study Status

Record Verification Date
January 2015
Overall Recruitment Status
Unknown status
Study Start Date
June 2013 (undefined)
Primary Completion Date
December 2015 (Anticipated)
Study Completion Date
December 2016 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Shanghai Pulmonary Hospital, Shanghai, China
Collaborators
Shanghai Center for Disease Control and Prevention, Jiangsu Province Centers for Disease Control and Prevention, Zhejiang University, Centers for Disease Control and Prevention

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Multi-center, prospective study is performed to investigate the efficacy of new short-course regimen for retreatment pulmonary tuberculosis patients. To obtain optimized short-course regimen, decrease treatment cost and improve success rate.
Detailed Description
China is the country with the second highest Tuberculosis (TB) burden in the world. Most of the retreatment TB patients may develop multi-drug resistant. The resistant rate of any of the anti-TB drug is 35.9%, and the multi-drug resistant rate is 15.4%. Retreatment TB becomes one of the factors which inhibit the decrease of morbidity and mortality of TB. It is also a tuff work in TB control. At present the standardized regimen for retreatment TB is 2SHREZ/6HRE or 3HREZ/6HRE. The drugs in the regimen are all first-line anti-TB drugs which are unsuitable for the high drug resistance prevalence, because the cure rate of this regimen is low and the adverse reaction is severe. Our study is a national multi-center, prospective trail to investigate the efficacy of a new super-short regimen for retreatment TB patients. The new regimen consists of 5 drugs lasting 5 months. The cure rate and success rate of the new regimen is compared with standardized regimen usually 8-9 months in order to obtain the optimized regimen.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Reinfection Pulmonary Tuberculosis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
864 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
arm A: super-short retreatment regimen
Arm Type
Experimental
Arm Description
A regimen of 5 drugs is to be administered. Isoniazid Aminosalicylate Tablets,0.3g tid po for 5 mon moxifloxacin tab, 0.4g qd po for 5 mon rifabutin capsule,0.3g qd po for 5 mon ethambutol tab, 0.75g qd po for 5 mon pyrazinamide tab, 0.5g tid po for 5 mon
Arm Title
arm B:standardized retreatment regimen
Arm Type
Active Comparator
Arm Description
8-9 months of standardized regimen is to be administered. regimen 1.2SHREZ/6HRE streptomycin injectable,0.75g qd intramuscular for 2 mon isoniazid tab,0.3g qd po for 8 mon rifampicin capsule,0.45-0.6g po for 8 mon ethambutol tab, 0.75g qd po for 8 mon pyrazinamide tab, 0.5g tid po for 2 mon or regimen 2.3HREZ/6HRE isoniazid tab,0.3g qd po for 9 mon rifampicin capsule,0.45-0.6g po for 9 mon ethambutol tab, 0.75g qd po for 9 mon pyrazinamide tab, 0.5g tid po for 3 mon
Intervention Type
Drug
Intervention Name(s)
Isoniazid Aminosalicylate Tablets
Other Intervention Name(s)
ethambutol tablets, pyrazinamide tablets, rifabutin capsules, moxifloxacin tablets
Intervention Description
a regimen consists of 5 anti-TB drugs (Isoniazid Aminosalicylate Tablets+pyrazinamide tablets+ethambutol tablets+rifabutin capsules+moxifloxacin tablets)to treat retreatment pulmonary tuberculosis patients. The total treatment course is 5 months.
Intervention Type
Drug
Intervention Name(s)
Streptomycin injectable
Other Intervention Name(s)
isoniazid tablets, ethambutol tablets, rifampicin capsules, pyrazinamide tablets
Intervention Description
standardized regimen 2 months of streptomycin injectable + isoniazid tablets + ethambutol tablets + rifampicin capsules + pyrazinamide tablets and 6 months of isoniazid tablets + ethambutol tablets + rifampicin capsules or 3 months of isoniazid tablets + ethambutol tablets + rifampicin capsules + pyrazinamide tablets and 6 months of isoniazid tablets + ethambutol tablets + rifampicin capsules to treat Arm B patients as a control to arm A.The treatment course is 8-9 months.
Primary Outcome Measure Information:
Title
success rate
Time Frame
for arm A,the point is 5 month after treatment. For arm B,the time point is at the end of the 8 or 9 month's treatment.
Secondary Outcome Measure Information:
Title
adverse reaction rate
Time Frame
for arm A,the point is 5 month after treatment. For arm B,the time point is at the end of the 8 or 9 month's treatment.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Sputum confirmed diagnosis of retreatment pulmonary tuberculosis Must be able to swallow tablets Must be able to sign written informed consent form Exclusion Criteria: Extra-pulmonary tuberculosis Diabetes Allergy to any of the medications in the regimen or pregnancy Liver disease Renal disease Metabolic disease Immune system disease Hematological disease Nervous system and mental disease Endocrine disease Malignant disease Receiving immunosuppressive therapy HIV/AIDS Alcohol addiction
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Qing Zhang, M.D
Phone
8621-65115006
Ext
2002
Email
zhqi709851@sohu.com
First Name & Middle Initial & Last Name or Official Title & Degree
Wei Sha, M.D
Phone
8621-65115006
Ext
2017
Email
shfksw@126.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Heping Xiao, M.D
Organizational Affiliation
Shanghai Pulmonary Hospital,China
Official's Role
Principal Investigator
Facility Information:
Facility Name
Shanghai Pulmonary Hospital
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200433
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Qing Zhang, M.D
Phone
8621-65115006
Ext
2002
Email
zhqi709851@sohu.com
First Name & Middle Initial & Last Name & Degree
Wei Sha, M.D
Phone
8621-65115006
Ext
2017
Email
shfksw@126.com
First Name & Middle Initial & Last Name & Degree
Qing Zhang, M.d

12. IPD Sharing Statement

Citations:
PubMed Identifier
29519716
Citation
Yan L, Kan X, Zhu L, Xu K, Yin J, Jie L, Li Y, Yue J, Cui W, Du J, Wang L, Tan S, Jiang X, Zeng Z, Xu S, Wang L, Chen Y, He W, Gao X, Bai D, Zhao C, Yan X, Zhu Y, Fan Y, Xie L, Deng A, Zhang Q, Xiao H. Short-course Regimen for Subsequent Treatment of Pulmonary Tuberculosis: A Prospective, Randomized, Controlled Multicenter Clinical Trial in China. Clin Ther. 2018 Mar;40(3):440-449. doi: 10.1016/j.clinthera.2018.01.013. Epub 2018 Mar 6.
Results Reference
derived

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Research on New Regimens for Retreatment Pulmonary Tuberculosis

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