College of Clinical Medicine, Chengdu University of Traditional Chinese Medicine.
Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan Province, P.R. China.
Medicine (Baltimore). 2021 Feb 5;100(5):e23915. doi: 10.1097/MD.0000000000023915.
In recent years, the incidence of ulcerative colitis (UC) is on the rise, and most of them are young adults. As the peak of the disease overlaps with the childbearing age, it has a great impact on the fertility of female patients. We, therefore, conduct a randomized and controlled trial to evaluate the efficacy and safety of mesalazine enteric-coated tablets combined with Kangfuxin Liquid (KFX) enema for the child-bearing period female with active UC.
In this randomized controlled study, a total of 236 eligible patients will be assigned to the experimental group (n = 118) or the control group (n = 118) in a 1:1 ratio. The control group will be taken mesalazine enteric-coated tablets combined with placebo enema and the experimental group will be taken mesalazine enteric-coated tablets combined with KFX enema. Participants will receive 8 weeks of intervention treatment and 3 months of maintenance treatment before pregnancy. The primary assessment is the Mayo score. Secondary outcomes include mucosal healing, faecal calprotectin (FC), Inflammatory Bowel Disease Quality (IBDQ), and pregnancy outcome.
This study will provide evidence regarding the efficacy and safety of KFX enema used before pregnancy on halting active UC, reducing the relapse rate during pregnancy, improving pregnancy outcome, and the quality of life.
Chinese Clinical Trials Register identifier, ChiCTR2000039161, registered on October 20, 2020.
近年来,溃疡性结肠炎(UC)的发病率呈上升趋势,且多数为青壮年。由于疾病的高峰期与生育年龄重叠,对女性患者的生育能力影响较大。因此,我们进行了一项随机对照试验,以评估美沙拉嗪肠溶片联合康复新液灌肠对活动期 UC 育龄期女性的疗效和安全性。
在这项随机对照研究中,将 236 名符合条件的患者按照 1:1 的比例随机分配到实验组(n=118)或对照组(n=118)。对照组给予美沙拉嗪肠溶片联合安慰剂灌肠,实验组给予美沙拉嗪肠溶片联合康复新液灌肠。参与者将接受 8 周的干预治疗和怀孕前 3 个月的维持治疗。主要评估指标为 Mayo 评分。次要结局包括黏膜愈合、粪便钙卫蛋白(FC)、炎症性肠病生活质量(IBDQ)和妊娠结局。
本研究将为康复新液灌肠在孕前用于停止活动期 UC、降低孕期复发率、改善妊娠结局和生活质量提供疗效和安全性的证据。
中国临床试验注册中心,ChiCTR2000039161,于 2020 年 10 月 20 日注册。