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DOI 10.1016/j.phymed.2026.157991

Медицинская библиотека · Phytomedicine : international journal of phytotherapy and phytopharmacology · 2026

Congrong Runtong oral liquid for functional constipation: A multicenter, placebo-controlled phase II trial.

Zhao Luqing, Sun Xiaohong, Zhu Lei, Chen Bin, Qin Danping, Fang Shengquan, Gao Jihua, Liu Chaoxia, Wu Hao, Liu Fei, Shen Danlei, Zhao Lu, Zhang Shengsheng

СтатьяМногоцентровое исследованиеРандомизированное исследованиеКлиническое исследование II фазыПеревод пока не подготовлен

Аннотация

BACKGROUND

This study aimed to evaluate the efficacy and safety of Congrong Runtong Oral Liquid (CROL) in treating functional constipation of Yang-deficiency type in adults.

OBJECTIVE

To determine the efficacy of Congrong Runtong Oral Liquid (CROL) versus placebo in adults with functional constipation of Yang-deficiency type.

METHODS

In this multicenter, double-blind, placebo-controlled randomized clinical trial, 180 participants aged 18-70 years, diagnosed with functional constipation meeting the Rome IV and Yang-deficiency type TCM criteria, were randomized 1:1:1 to receive CROL (3 g or 6g/day) or placebo for 8 weeks. The primary outcome was treatment response (≥ 3 complete spontaneous bowel movements [CSBMs] per week plus increase of ≥ 1 CSBMs per week from baseline for ≥ 4 weeks during the 8-week treatment period). Secondary outcomes included CSBMs, spontaneous bowel movements [SBMs], fecal characteristics, stool passage difficulty, PAC-QOL scores, rescue medication use and adverse events. Outcomes were assessed over 8 weeks.

RESULTS

Among participants (mean age 44.5 years; 80% female), the response rate was 60.7% (37/61) with 6g/d CROL, 35.0% (21/60) with 3g/d CROL, and 18.6% (11/59) with placebo (p < 0.0001 for 6g/d vs placebo; p = 0.044 for 3g/d vs placebo). Weekly CSBMs were 2.0 (1.3) (6g/d), 1.5 (1.4) (3g/d), and 1.2 (1.2) (placebo) (p = 0.001 for 6g/d vs placebo). There was no statistically significant difference in weekly SBMs among the three groups, although the 6g/d CROL group showed a numerical trend toward higher SBMs (3.7 [1.9]) compared with the placebo group (3.1 [1.8], p = 0.0735). The rate of treatment-related AEs was 1.6% in the 6g/day group, 0.0% in the 3g/day group, and 3.4% in the placebo group, respectively (p = 0.3241). No severe events were reported.

CONCLUSION

CROL was effective and well-tolerated in adult patients with functional constipation of the Yang-deficiency type.

REGISTRATION NUMBER: NCT05803161.

Для цитирования: Zhao Luqing, Sun Xiaohong, Zhu Lei, Chen Bin, Qin Danping, Fang Shengquan, Gao Jihua, Liu Chaoxia, Wu Hao, Liu Fei, Shen Danlei, Zhao Lu, Zhang Shengsheng. Congrong Runtong oral liquid for functional constipation: A multicenter, placebo-controlled phase II trial.. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2026. DOI: 10.1016/j.phymed.2026.157991.

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