The Prophylaxis of Tuberculosis According to TSPOT Results After Kidney Transplantation (PTTKT):Protocol for an Open-label, Prospective, Randomized, 3-arm, Controlled Trial
试验速览
- 阶段
- 不适用
- 入组人数
- 303
- 主要终点
- The primary outcome is the incidence of tuberculosis in these groups.
研究概览
简要总结
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.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 65 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •living-donor kidney transplantation;
- •eGFR level > 45ml/min/1.73m2 at discharge;
- •18<Age <65years;
- •receiving standard triad immunosuppressive regimen
排除标准
- •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
研究组 & 干预措施
Positive TSPOT results with clinical risk factors group
patients receive isoniazid 300mg once daily for six months after kidney transplant surgery form discharge
干预措施: Isoniazid (Drug)
Negative TSPOT results with clinical risk factors group
patients receive no additional therapy
干预措施: without any additional anti-tuberculosis treatment (Other)
Clinical risk factors group
patients receive isoniazid 300mg once daily for six months after kidney transplant surgery form discharge
干预措施: Isoniazid (Drug)
结局指标
主要结局
The primary outcome is the incidence of tuberculosis in these groups.
时间窗: 12 months
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.
次要结局
- The secondary outcome is subject incidence of adverse events(12 months)
研究者
Tao Lin
Professor Tao Lin
West China Hospital
