Neudecker Jens, Malzahn Uwe, Heuschmann Peter, Behrens Uwe, Walles Thorsten
Department of General, Visceral, Vascular and Thoracic Surgery, Surgical Regional Centre Berlin of CHIR-Net, Charité University Medicine Berlin, Campus Charité Mitte, Charitéplatz 1, 10117, Berlin, Germany.
Clinical Trial Center Würzburg (CTCW), University Hospital Würzburg, Josef-Schneider Strasse 2, 97080, Würzburg, Germany.
Trials. 2015 Nov 30;16:540. doi: 10.1186/s13063-015-1060-z.
For the surgical treatment of recurrent primary spontaneous pneumothoraces (rPSP) different operative therapies are applied to achieve permanent freedom from recurrence.
METHODS/DESIGN: This multicenter clinical trial evaluates the long-term results of two commonly applied surgical techniques for the treatment of rPSP. Based on the inclusion and exclusion criteria, and after obtaining the patients' informed consent, participants are randomized into the two surgical treatment arms: pulmonary wedge resection plus parietal pleurectomy (WRPP) or parietal pleurectomy alone (PP). Consecutively, all study participants will be followed up for two years to evaluate the surgical long-term effect. The primary efficacy endpoint is the recurrence rate of pneumothorax within 24 months after surgery. The calculated sample size is 360 patients (n = 180 per treatment arm) to prove superiority of one of the two treatments. So far, 22 surgical sites have submitted their declaration of commitment, giving the estimated number of participating patients.
A prospective randomized clinical trial has been started to compare two established surgical therapies to evaluate the long-term results regarding recurrence rates. Furthermore, cost of treatment, and influence on the perioperative morbidity and mortality as well as on quality of life are analyzed. If the study reveals equivalence for both surgical techniques, unnecessary pulmonary resections could be avoided.
ClinicalTrials gov: NCT01855464 , 06.05 2013.
对于复发性原发性自发性气胸(rPSP)的外科治疗,采用了不同的手术疗法以实现永久性无复发。
方法/设计:这项多中心临床试验评估了两种常用于治疗rPSP的手术技术的长期效果。根据纳入和排除标准,并在获得患者知情同意后,将参与者随机分为两个手术治疗组:肺楔形切除术加胸膜顶剥脱术(WRPP)或单纯胸膜顶剥脱术(PP)。随后,对所有研究参与者进行为期两年的随访,以评估手术的长期效果。主要疗效终点是术后24个月内气胸的复发率。计算得出的样本量为360例患者(每个治疗组n = 180例),以证明两种治疗方法中一种的优越性。到目前为止,已有22个手术地点提交了参与承诺声明,给出了预计参与患者的数量。
已启动一项前瞻性随机临床试验,比较两种既定的手术疗法,以评估复发率方面的长期效果。此外,还分析了治疗成本、对围手术期发病率和死亡率以及生活质量的影响。如果研究表明两种手术技术等效,则可以避免不必要的肺切除术。
ClinicalTrials gov:NCT01855464,2013年5月6日。