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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
West China Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Kidney Transplant Infection

Eligibility Criteria

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

Inclusion Criteria:

  1. living-donor kidney transplantation;
  2. eGFR level > 45ml/min/1.73m2 at discharge;
  3. 18<Age <65years;
  4. receiving standard triad immunosuppressive regimen

Exclusion Criteria:

  1. alanine aminotransferase (ALT) or aspartate aminotransferase (AST) > 2.5 or more of upper limit of normal
  2. Combined with HBV/HCV/HIV/TB infection in the donor or recipient;
  3. Malignancy history in the donor and recipient;
  4. organ transplant history in the recipient.
  5. 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

    First Posted
    October 19, 2021
    Last Updated
    March 21, 2022
    Sponsor
    West China Hospital
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    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
    background
    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
    background

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    The Prophylaxis of Tuberculosis According to TSPOT Results After Kidney Transplantation

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