Obstetrics and Gynaecology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Obstetrics and Gynaecology, Shenzhen Second People's Hospital, Shenzhen, Guangdong, China.
BMJ Open. 2021 Oct 18;11(10):e044347. doi: 10.1136/bmjopen-2020-044347.
Leiomyoma recurrence is a major concern for long-term myomectomy management, especially for multiple leiomyomas. Gonadotropin-releasing hormone agonist (GnRHa) is one of the most effective medications to reduce the volume of fibroids and the uterus. However, its role in preventing recurrence after conservative surgery remains unclear. At present, there is no randomised clinical trial determining the efficacy of GnRHa treatment for preventing multiple leiomyomas recurrence after myomectomy.
We are conducting a phase IV randomised controlled trial in women aged 18-45 undergoing myomectomy for multiple leiomyomas. After surgery, women whose pathological result confirms multiple leiomyomas are randomised in a 1:1 ratio into an observation or GnRHa group. The primary outcome is the recurrence of either clinical symptoms or fibroids on imaging. Patients will be assessed for adverse events during the follow-up.
The study was approved by the Medical Ethics Committee of the Tongji Hospital Affiliated with the Tongji Medical College of Huazhong University of Science and Technology (TJ-IRB20180311) according to the submitted study protocol (V.1.0, 10 November 2017) and informed consent (V.1.0, 10 November 2017). The results will be presented at domestic and international conferences and published in peer-reviewed journals.
ChiCTR-IPR-17012992.
子宫肌瘤复发是长期子宫肌瘤切除术管理的主要关注点,尤其是多发性子宫肌瘤。促性腺激素释放激素激动剂(GnRHa)是一种最有效的药物,可以减少肌瘤和子宫的体积。然而,其在预防保守性手术后复发的作用尚不清楚。目前,尚无随机临床试验确定 GnRHa 治疗在预防子宫肌瘤切除术后多发性子宫肌瘤复发中的疗效。
我们正在对因多发性子宫肌瘤接受子宫肌瘤切除术的 18-45 岁女性进行一项四期随机对照试验。手术后,病理结果证实为多发性子宫肌瘤的女性按 1:1 的比例随机分为观察组或 GnRHa 组。主要结局是影像学上出现临床症状或肌瘤复发。患者在随访期间将被评估不良事件。
该研究根据提交的研究方案(V.1.0,2017 年 11 月 10 日)和知情同意书(V.1.0,2017 年 11 月 10 日),经华中科技大学同济医学院附属同济医院医学伦理委员会批准(TJ-IRB20180311)。结果将在国内和国际会议上进行报告,并发表在同行评议的期刊上。
ChiCTR-IPR-17012992。