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临床试验/NCT05707702
NCT05707702撤回3 期

Lactobacillus Lozenges as Preventative Care in Low-grade Dysplasia

Boston Medical Center2 个研究点 分布在 1 个国家开始时间: 2024年4月29日最近更新:
适应症

试验速览

阶段
3 期
状态
撤回
试验地点
2
主要终点
Clinical regression of dysplastic lesion

研究概览

简要总结

There are limited evidence-based management options for patients with low-grade oral dysplasia. Despite the risk of malignant transformation, management is frequently limited to risk factor reduction (such as smoking cessation) and clinical surveillance. An intervention for low-grade oral dysplasia which could induce regression or decrease rates of malignant transformation has the potential to be a valuable preventative tool to reduce rates of oral cancer.

The investigators will conduct a randomized clinical trial to investigate if the administration of a probiotic lozenge to patients with low-grade oral dysplasia result in decreased peri-tumoral inflammation as evidenced by impacts on populations of tumor-associated macrophages and tumor-infiltrating lymphocytes, and decreased dysbiosis at the disease site compared with the contralateral normal site. The investigators hypothesize that these changes may increase the rate of clinical regression of these lesions.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Outcomes Assessor)

入排标准

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

入选标准

  • Presence of biopsy-proven low-grade or mild oral dysplasia

排除标准

  • Active oral cavity malignancy
  • Active oral cavity high grade dysplasia
  • Currently undergoing chemotherapy or immunotherapy, or have used these agents within the prior 6 months
  • History of external beam radiation therapy to the head and neck area
  • Diagnosis of HIV with decreased CD4 count and/or detectable viral load
  • Current use of systemic or orally absorbed steroids
  • Patient undergoing stem cell transplantation
  • Patients taking anti-rejection medication after stem cell or solid organ transplantation
  • Patients using injectable immunosuppressive drugs for autoimmune disease
  • Pregnant or nursing women
  • Patients who are hospitalized
  • Patients with a heart valve abnormalities or a history of valve replacement or endocarditis
  • Patients with active severe acute intestinal disease (active bowel leak, acute abdomen, active colitis) or a history of short bowel syndrome

结局指标

主要结局

Clinical regression of dysplastic lesion

时间窗: 6 weeks

This outcome will be assessed using blinded review of clinical photographs and measurements of the lesions to determine if the lesion has regressed, remained the same or progressed since baseline.

次要结局

  • Oral dysplasia lesions at 12 weeks(12 weeks)
  • Microbiome at the lesion site(baseline, 6 weeks, 12 weeks)
  • Change in peri-tumoral inflammation(baseline, 6 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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