跳至主要内容
临床试验/NCT06571097
NCT06571097招募中不适用

Levofloxacin in the Treatment of Chronic Functional Constipation Associated With PIB Infection: A Multi-center, Exploratory Clinical Study

Haifeng Lan1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2024年7月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
50
试验地点
1
主要终点
Total effective rate of levofloxacin in the treatment of chronic functional constipation.

研究概览

简要总结

Constipation, a prevalent clinical condition, significantly impacts patients' quality of life, yet relevant clinical trial technical guidelines have yet to be issued domestically. This disease encompasses various classifications based on etiology, pathology, and pathophysiological characteristics. Slow transit constipation (STC), specifically, arises from colonic motility disorders and is recognized as a neuromuscular colonopathy. Currently, limited therapeutic options are available for patients with refractory STC, rendering it a common ailment associated with substantial disease burden and uncertain etiology. Consequently, identifying the cause and developing effective, targeted, and safe treatment strategies is of paramount importance.

Our research team has made a groundbreaking international discovery, revealing that STC is caused by infection with a novel Shigella-like bacterium, termed the peristaltic contraction-inhibiting bacterium (PIB), which secretes docosapentaenoic acid (DPA), an unsaturated fatty acid. The pathogenic mechanism involves inhibition of intestinal peristalsis, subsequently slowing colonic transit. Preliminary epidemiological studies confirm the exclusive presence of PIB in feces from patients with intractable constipation, whereas it is virtually absent in healthy individuals. Notably, consumption of high-dose DPA does not affect colonic transit or induce constipation; however, intracolonic administration does.

In response to PIB-induced STC, our team screened a range of antibiotics and identified two primary classes with potent antibacterial effects against PIB: fluoroquinolones and carbapenems. Both classes exhibit strong inhibitory activity against PIB, suggesting their potential use in chronic constipation treatment. Levofloxacin, a quinolone antibiotic, possesses broad-spectrum and potent antibacterial properties, effective in treating intestinal and urinary tract infections. Given that PIB has been confirmed as a novel Shigella-like species, and quinolones are established as the first-line antibiotics for Shigella infections, levofloxacin's efficacy against PIB was anticipated. Preliminary studies have validated levofloxacin's ability to inhibit PIB growth, thereby alleviating PIB-induced refractory constipation through sensitivity testing.

The primary objective of this study is to utilize levofloxacin to suppress PIB, thereby achieving the relief of chronic functional constipation.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Participants must meet all of the following criteria to enter the trial.
  • •Signed written informed consent;
  • •Diagnosed chronic functional constipation according to Rome III or IV criteria, and infected with PIB;
  • •Patients who have not taken other types of antibiotics in the past 1 month;
  • •Bowel organic lesions (tumors and severe inflammatory lesions, etc.) were excluded by colonoscopy in the past 2 years.
  • •The subjects could follow the follow-up plan, objectively describe the symptoms, and cooperate with the completion of the scale; 7)Agree to maintain similar diet and activity levels from the screening visit to the end of the study;

排除标准

  • •Exclusion criteria: Subjects must exclude all of the following conditions to enter the study.
  • •Pregnant and lactating women;
  • •Patients with drug-induced constipation, including constipation induced by opioids and antidepressants;
  • •During the study period, changes in lifestyle and dietary habits are not recommended in principle;
  • •Patients with diseases that affect the conduct or results of the study, such as mental illness, serious cardiopulmonary, liver and kidney diseases, history of gastrointestinal surgery, epilepsy, etc.
  • •Those who cannot take samples and complete inspection items as required;
  • •Allergic to levofloxacin; 7)Other researchers found it inappropriate to participate in the project for clinical manifestations or diseases.

研究组 & 干预措施

Levofloxacin

Experimental

Levofloxacin: 0.5g(500mg)/day for 2 weeks

干预措施: Levofloxacin (Drug)

结局指标

主要结局

Total effective rate of levofloxacin in the treatment of chronic functional constipation.

时间窗: 6 months

Obvious effect: no defecation difficulty, the number of spontaneous defecation ≥3 times/week (no effort and time consuming when defecating, no feeling of inadequate defecation, normal stool characteristics, etc.); Effective: the difficulty of defecation is improved than before, and the number of autonomous defecation is not less than 3 times/week (one of the time-consuming and laborious defecation or improper defecation or abnormal stool characteristics occurs during defecation);Ineffective: The difficulty of defecation is no better than before, and the number of spontaneous defecation is less than 3 times/week.Total effective rate = (significant efficiency + effective rate) Number of cases/total number of cases ×100%.

次要结局

  • Bristol scale(6 months)
  • PIB concentration (DPA content of docosapentaenoic acid)(6 months)
  • The incidence of serious adverse events(6 months)
  • Proportion of patients with first defecation(24-48 hours)
  • Time of first defecation(24-48 hours)
  • Number of frequency of use of rescue drugs and other Other defecation medications per week(6 months)
  • PAC-SYM(6 months)
  • PAC-QoL scale(6 months)
  • Patient satisfaction with treatment survey(6 months)

研究者

发起方
Haifeng Lan
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Haifeng Lan

student

Nanjing Medical University

研究点 (1)

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