Institute of Medical Microbiology and Hospital Hygiene, Faculty of Medicine, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Institute of Medical Microbiology and Hospital Hygiene, Faculty of Medicine, Otto-von-Guericke University, Leipziger Str. 44, 39120, Magdeburg, Germany.
Trials. 2020 Feb 12;21(1):175. doi: 10.1186/s13063-020-4102-0.
SABATO (Staphylococcus aureus bacteremia antibiotic treatment options) is a randomized, parallel-group, clinical non-inferiority trial designed to examine the efficacy and safety of early oral switch therapy in low-risk Staphylococcus aureus infection. The original trial protocol was published in Trials (accessible at https://doi.org/10.1186/s13063-015-0973-x ). Here we describe final amendments to the study protocol and discuss the underlying rationale.
METHODS/DESIGN: Three major changes were introduced into the study protocol: (1) the inclusion and exclusion criteria were refined so that patients with certain comorbidities (end-stage renal disease, severe liver disease) and uninfected foreign bodies (orthopedic prosthesis, pacemaker, implanted cardiac cardioverter-defibrillator) became eligible for enrollment under certain conditions; (2) the target sample size was decreased by choosing a conventional non-inferiority margin of 10% and converting the interim analysis (215 patients) into the final analysis; and (3) an additional follow-up visit after 30 days was introduced to allow for a closer follow-up of patients.
Changes to the study protocol were introduced to improve the enrollment and follow-up of patients. Furthermore, the decrease of the sample size will facilitate completion of the trial.
ClinicalTrials.gov, NCT01792804. Registered on 13 February 2013. German Clinical trials register, DRKS00004741. Registered on 4 October 2013, EudraCT 2013-000577-77.
SABATO(金黄色葡萄球菌菌血症抗生素治疗选择)是一项随机、平行组、临床非劣效性试验,旨在研究低危金黄色葡萄球菌感染早期口服转换治疗的疗效和安全性。原始试验方案发表在 Trials 上(可在 https://doi.org/10.1186/s13063-015-0973-x 访问)。在这里,我们描述了对研究方案的最终修订,并讨论了其基本原理。
方法/设计:研究方案引入了三项重大变更:(1)纳入和排除标准进行了细化,以便在某些条件下,患有某些合并症(终末期肾病、严重肝病)和无感染的异物(骨科假体、起搏器、植入式心脏除颤器)的患者符合入组条件;(2)选择常规的非劣效性边界 10%,并将中期分析(215 例患者)转换为最终分析,从而降低了目标样本量;(3)增加了 30 天后的随访访视,以便更密切地随访患者。
对研究方案进行了变更,以改善患者的入组和随访。此外,样本量的减少将有助于试验的完成。
ClinicalTrials.gov,NCT01792804。于 2013 年 2 月 13 日注册。德国临床试验注册处,DRKS00004741。于 2013 年 10 月 4 日注册,EudraCT 2013-000577-77。