Mokhtari Gholamreza, Teimoori Mojtaba
Transplant surgeon, Urology Research Center, Razi Hospital, Guilan University of Medical Sciences, Rasht, Guilan, Iran.
Urology Department, Guilan University of Medical Sciences, Rasht, Guilan, Iran.
Trials. 2018 Jun 28;19(1):345. doi: 10.1186/s13063-018-2744-y.
Kidney transplantation is the best strategy for the management of end-stage renal disease; however, the outcomes need to improve further. Macrolides show antimicrobial and anti-inflammatory properties in chronic diseases and intraoperatively, and can accumulate in tissues for extended periods. Therefore, theoretically, when administered to a donor and because of accumulation in the donor kidney, macrolides can cause graft immunomodulation and improve kidney transplantation outcomes.
This study is a single-center, randomized clinical trial. A total of 60 kidney donors will be randomly allocated to the azithromycin or placebo group and treated with a single dose (1 g) of azithromycin or placebo, respectively, 1 day before surgery. Recruitment commenced in September 2016 and is expected to be completed by March 2018. The primary outcome is kidney graft function. The secondary outcomes include rejection rate, urinary tract infections in graft recipients, pain and systemic inflammatory response syndrome in live donors, and complications in both donors and recipients. Outcomes will be evaluated at baseline and every day in the first week after transplantation, as well as at 1 and 3 months post transplantation. Adverse reactions will be documented. If the efficacy of azithromycin in reducing adverse outcomes is confirmed, it would serve as an easy to use, economic intervention able to lower post-transplantation risks.
Short and mid-term analyses of blood and urine samples as well as immunological assays will facilitate a more in-depth analysis of the effects of azithromycin on transplantation outcomes.
Iranian Clinical Trial Registry, IRCT201606141853N11 , registered on September 5, 2016.
肾移植是终末期肾病治疗的最佳策略;然而,其治疗效果仍需进一步改善。大环内酯类药物在慢性疾病及手术过程中具有抗菌和抗炎特性,且能在组织中长时间蓄积。因此,从理论上讲,给供体使用大环内酯类药物后,由于其在供体肾脏中的蓄积,可引起移植物免疫调节并改善肾移植效果。
本研究为单中心随机临床试验。总共60名肾供体将被随机分配至阿奇霉素组或安慰剂组,分别在手术前1天接受单剂量(1克)阿奇霉素或安慰剂治疗。招募工作于2016年9月开始,预计2018年3月完成。主要结局指标为肾移植功能。次要结局指标包括排斥反应发生率、移植受者的尿路感染、活体供者的疼痛及全身炎症反应综合征,以及供者和受者的并发症。将在基线时、移植后第一周每天以及移植后1个月和3个月评估结局。记录不良反应。如果阿奇霉素在降低不良结局方面的疗效得到证实,它将成为一种易于使用且经济的干预措施,能够降低移植后风险。
对血液和尿液样本进行短期和中期分析以及免疫测定,将有助于更深入地分析阿奇霉素对移植结局的影响。
伊朗临床试验注册中心,IRCT201606141853N11,于2016年9月5日注册。