The Prophylaxis of Tuberculosis According to TSPOT Results After Kidney Transplantation (PTTKT)
Primary Purpose
Kidney Transplant Infection, Tuberculosis, Isoniazid Toxicity
Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Isoniazid
without any additional anti-tuberculosis treatment
Sponsored by
About this trial
This is an interventional prevention trial for Kidney Transplant Infection
Eligibility Criteria
Inclusion Criteria:
- living-donor kidney transplantation;
- eGFR level > 45ml/min/1.73m2 at discharge;
- 18<Age <65years;
- receiving standard triad immunosuppressive regimen
Exclusion Criteria:
- alanine aminotransferase (ALT) or aspartate aminotransferase (AST) > 2.5 or more of upper limit of normal
- Combined with HBV/HCV/HIV/TB infection in the donor or recipient;
- Malignancy history in the donor and recipient;
- organ transplant history in the recipient.
- The positive TSPOT result or past TB history in the donor
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Placebo Comparator
Experimental
Arm Label
Positive TSPOT results with clinical risk factors group
Negative TSPOT results with clinical risk factors group
Clinical risk factors group
Arm Description
patients receive isoniazid 300mg once daily for six months after kidney transplant surgery form discharge
patients receive no additional therapy
patients receive isoniazid 300mg once daily for six months after kidney transplant surgery form discharge
Outcomes
Primary Outcome Measures
The primary outcome is the incidence of tuberculosis in these groups.
The primary objective of this study is to evaluate the incidence of tuberculosis between these groups. The incidence of tuberculosis was assessed by WHO TB guidelines 2021.
Secondary Outcome Measures
The secondary outcome is subject incidence of adverse events
The primary objective of this study is to evaluate the safety of isoniazide among the kidney transplant recipients
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT05249699
Brief Title
The Prophylaxis of Tuberculosis According to TSPOT Results After Kidney Transplantation
Acronym
PTTKT
Official Title
The Prophylaxis of Tuberculosis According to TSPOT Results After Kidney Transplantation (PTTKT):Protocol for an Open-label, Prospective, Randomized, 3-arm, Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
March 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
April 1, 2022 (Anticipated)
Primary Completion Date
July 1, 2023 (Anticipated)
Study Completion Date
August 1, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
West China Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Organ transplant recipients are a high incidence group of tuberculosis infection, and the incidence rate is 7-27 times that of the general population. The prevention of postoperative tuberculosis infection is an important part of kidney transplant recipients postoperative follow-up. Taking reasonable tuberculosis prevention strategies for organ transplant recipients can better prevent the occurrence of postoperative tuberculosis and reduce the unreasonable use of anti-tuberculosis drugs. The previous screening methods for active tuberculosis mainly include sputum smear culture, tissue biopsy, tuberculin skin test, tuberculosis antibody, tuberculosis DNA, and chest imaging. However, there is still a lack of accurate and effective means for screening for latent tuberculosis infection. The tuberculosis interferon-γ release test has recently received more and more attention as a means of screening for potential tuberculosis infection. However, how to apply tuberculosis interferon-γ release test in clinical practice is still controversial. The investigators hope to explore the clinical application prospects and practical value of tuberculosis interferon-γ release test through this research.
According to the conclusion of the retrospective study, the investigators found that the recipients with negative TSPOT result maybe don't need follow the isoniazid treatment to prevent the development of tuberculosis even though participants have clinical risk factor of tuberculosis(include past tuberculosis history, the close contact with active tuberculosis patients, an area with a high incidence of tuberculosis, abnormal chest x ray performance ).
The investigators will divided the recipients with tuberculosis risk factors into three groups randomly. Of course, the invention require written informed consent. The first group with positive tuberculosis interferon gamma release assay (TSPOT) result will follow through with the treatment ,which is a daily dose of isoniazid for six months(300mg daily) after kidney transplant surgery. The second group with negative TSPOT result will not follow through the isoniazid treatment. The third group will follow through with the isoniazid treatment no matter their TSPOT results. The investigators will conduct a prospective clinical trial with the first aim of exploring the effectiveness of TSPOT results in kidney transplant recipients with clinical tuberculosis risk factors, and the second aim of exploring the benefit of the isoniazid treatment follow the TSPOT results rather than clinical risk factors.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Kidney Transplant Infection, Tuberculosis, Isoniazid Toxicity
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
303 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Positive TSPOT results with clinical risk factors group
Arm Type
Experimental
Arm Description
patients receive isoniazid 300mg once daily for six months after kidney transplant surgery form discharge
Arm Title
Negative TSPOT results with clinical risk factors group
Arm Type
Placebo Comparator
Arm Description
patients receive no additional therapy
Arm Title
Clinical risk factors group
Arm Type
Experimental
Arm Description
patients receive isoniazid 300mg once daily for six months after kidney transplant surgery form discharge
Intervention Type
Drug
Intervention Name(s)
Isoniazid
Intervention Description
prevent the development of tuberculosis
Intervention Type
Other
Intervention Name(s)
without any additional anti-tuberculosis treatment
Intervention Description
reduce the number of Participants With Treatment-Related Adverse Events
Primary Outcome Measure Information:
Title
The primary outcome is the incidence of tuberculosis in these groups.
Description
The primary objective of this study is to evaluate the incidence of tuberculosis between these groups. The incidence of tuberculosis was assessed by WHO TB guidelines 2021.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
The secondary outcome is subject incidence of adverse events
Description
The primary objective of this study is to evaluate the safety of isoniazide among the kidney transplant recipients
Time Frame
12 months
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:
living-donor kidney transplantation;
eGFR level > 45ml/min/1.73m2 at discharge;
18<Age <65years;
receiving standard triad immunosuppressive regimen
Exclusion Criteria:
alanine aminotransferase (ALT) or aspartate aminotransferase (AST) > 2.5 or more of upper limit of normal
Combined with HBV/HCV/HIV/TB infection in the donor or recipient;
Malignancy history in the donor and recipient;
organ transplant history in the recipient.
The positive TSPOT result or past TB history in the donor
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
32610111
Citation
Kim H, Kim SH, Jung JH, Kim MJ, Kim H, Shin S, Chong YP, Kim YH, Lee SO, Choi SH, Kim YS, Woo JH, Park SK, Han DJ. The usefulness of quantitative interferon-gamma releasing assay response for predicting active tuberculosis in kidney transplant recipients: A quasi-experimental study. J Infect. 2020 Sep;81(3):403-410. doi: 10.1016/j.jinf.2020.06.070. Epub 2020 Jun 29.
Results Reference
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PubMed Identifier
32620949
Citation
Shu CC, Tsai MK, Lin SW, Wang JY, Yu CJ, Lee CY. Latent Tuberculosis Infection Increases in Kidney Transplantation Recipients Compared With Transplantation Candidates: A Neglected Perspective in Tuberculosis Control. Clin Infect Dis. 2020 Aug 14;71(4):914-923. doi: 10.1093/cid/ciz851.
Results Reference
background
PubMed Identifier
25608587
Citation
Kim SH, Lee SO, Park IA, Kim SM, Park SJ, Yun SC, Jung JH, Shin S, Kim YH, Choi SH, Kim YS, Woo JH, Park SK, Park JS, Han DJ. Isoniazid treatment to prevent TB in kidney and pancreas transplant recipients based on an interferon-gamma-releasing assay: an exploratory randomized controlled trial. J Antimicrob Chemother. 2015 May;70(5):1567-72. doi: 10.1093/jac/dku562. Epub 2015 Jan 20.
Results Reference
background
PubMed Identifier
21749641
Citation
Kim SH, Lee SO, Park JB, Park IA, Park SJ, Yun SC, Jung JH, Kim YH, Kim SC, Choi SH, Jeong JY, Kim YS, Woo JH, Park SK, Park JS, Han DJ. A prospective longitudinal study evaluating the usefulness of a T-cell-based assay for latent tuberculosis infection in kidney transplant recipients. Am J Transplant. 2011 Sep;11(9):1927-35. doi: 10.1111/j.1600-6143.2011.03625.x. Epub 2011 Jul 12. Erratum In: Am J Transplant. 2011 Nov;11(11):2541.
Results Reference
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The Prophylaxis of Tuberculosis According to TSPOT Results After Kidney Transplantation
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