Department of Gastroenterology, The Second Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine, Guangzhou, China.
Guangzhou University of Traditional Chinese Medicine, Guangzhou, China.
Ann Palliat Med. 2021 Apr;10(4):4897-4905. doi: 10.21037/apm-21-650.
With the changes in lifestyle and diet, the incidence and mortality of colorectal cancer (CRC) is increasing in China. CRC mainly develops from colorectal adenomas (CRAs). There is a lack of chemopreventative drugs with definite efficacy for CRAs. Tiaochang Xiaoliu Decoction (TXD) was developed by Professor Yunjian Luo and has been used clinically over the last ten years for the prevention of CRA recurrence. To facilitate its clinical use, TXD was further standardized and produced as "Tiaochang Xiaoliu Decoction Granules (TXDG)". A study was designed to investigate the preventive effects of TXDG on the recurrence of CRA.
A randomized, double-blinded, controlled, and multi-center experiment is proposed to assess the effectiveness and safety of TXDG. Patients with CRAs (after complete polypectomy under colonoscopy) will be randomly divided into two groups, one will be treated with TXDG (the TXDG group) and the other will be treated with a TXDG mimetic agent (the TXDG mimetic group). The patients will be treated for 6 months and followed up for 3 years. Follow-up colonoscopy is expected to be carried out within 1 to 3 years after the baseline examinations. The primary outcome measure is adenoma detection rate within 1 to 3 years. The secondary outcome measures are the number, location, and pathology of the adenomas, and the polyp detection rate.
Reliable objective evidence will be provided to evaluate the efficacy and safety of TXDG as an accessorial therapy for CRA occurrence in post-polypectomy patients.
ChiCTR2000035257.
随着生活方式和饮食结构的改变,中国结直肠癌(CRC)的发病率和死亡率呈上升趋势。CRC 主要由结直肠腺瘤(CRAs)发展而来。目前缺乏明确有效的 CRA 化学预防药物。调畅消瘤汤(TXD)由罗云坚教授开发,临床应用十余年,用于预防 CRA 复发。为便于临床应用,TXD 进一步规范化并制成“调畅消瘤汤颗粒(TXDG)”。本研究旨在探讨 TXDG 对 CRA 复发的预防作用。
拟采用随机、双盲、对照、多中心试验评估 TXDG 的有效性和安全性。CRAs 患者(结肠镜下息肉完全切除后)将被随机分为两组,一组给予 TXDG(TXDG 组)治疗,另一组给予 TXDG 模拟剂(TXDG 模拟剂组)治疗。患者治疗 6 个月,随访 3 年。预计在基线检查后 1 至 3 年内进行随访结肠镜检查。主要结局指标为 1 至 3 年内的腺瘤检出率。次要结局指标为腺瘤的数量、位置和病理以及息肉检出率。
将为 TXDG 作为息肉切除术后患者 CRA 发生的辅助治疗提供可靠的客观证据,评价其疗效和安全性。
ChiCTR2000035257。