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临床试验/NCT05525260
NCT05525260招募中2 期

A Randomized Phase II Trial of Limonene for Pulmonary Nodule Chemoprevention

Shanghai Jiao Tong University School of Medicine1 个研究点 分布在 1 个国家目标入组 160 人开始时间: 2023年2月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
160
试验地点
1
主要终点
Changes in the sum of longest diameters of target nodules (multiple nodules) between the drug group and the placebo group.

研究概览

简要总结

The prevention and treatment of lung nodules involves many fields in preventive medicine and clinical medicine. A nodule is a growth or lump that may be malignant (cancer) or benign (not cancer). This study is aim to investigate the chemopreventive effect of limonene in inhibiting the occurrence/progression of ground glass pulmonary nodules. It is expected that limonene can be used as a safe and effective chemopreventive agent for preventing the development/progress of pulmonary nodules as well as expanding the indications of limonene.

详细描述

Early prevention, early detection and early treatment of lung cancer can help reduce the incidence and improve the survival rate.Chemoprevention is known to have an important role in high-risk people because it has the potential to prevent or reverse the progression of lung cancer.Lung nodules are good targets for testing the efficacy of chemopreventive agents.So far,none of the chemopreventive agents have been shown to be effective.

Limonene is widely found in the essential oils of traditional Chinese medicine tangerine peel, green peel and other plants. Its taste is sour, sweet and pungent. It has an aromatic odor effect. Limonene Capsule, a Chinese patent medicine, has been on the market, which is suitable for the treatment of cholecystitis, cholangitis, cholelithiasis, and postoperative biliary syndrome.Preliminary studies of the research group suggest that it has a potential anti-cancer effect.

This randomized, double-blind, controlled trial studied limonene compared with placebo in treating high-risk patients with pure ground glass pulmonary nodules,so as to expand indications.

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
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
45 Years 至 75 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Non-smokers (those who have smoked less than 100 cigarettes in their lifetime, including those who have never smoked in their lifetime).
  • Subjects must have positive nodules detected by high-resolution CT(HRCT): longest diameter > 6 mm and < 20 mm; pure ground glass nodule; according to the judgment of the clinician, follow-up can be performed, and surgical excision is not recommended for the time being; the nodules did not disappear or were not significantly reduced by more than 2 mm after six months follow-up; subjects should have at least one positive nodule when had multiple nodules.
  • ECOG performance status 0-
  • Those who accept and are willing to sign the informed consent.

排除标准

  • Subjects with the history of autoimmune diseases and severe gastrointestinal diseases;
  • Subjects suffering from malignant tumor, severe heart disease, severe liver or kidney disease currently or within the past 5 years;
  • Within 6 weeks since prior herbal supplements, non-steroidal anti-inflammatory drugs, or antibiotics
  • Subjects who are allergic to limonene capsules or citrus foods;
  • Use of any other investigational agents at time of enrollment in the study during the three months preceding study enrollment
  • Pregnant or lactating females, or those who disagreeing with contraception;
  • Subjects who have a history of mental illness and cannot cooperate with this project;
  • HIV-positive subjects should be excluded.
  • Subjects whose organ and bone marrow function indexes exceeded the following range of normal value were excluded:
  • Leukocytes: 3.5-9.5 109/L;
  • Absolute neutrophil count: 1.8-6.3 109/L;
  • Platelets: 125-350 109/L;
  • Total bilirubin: 5.0-21.0 µmol /L;
  • AST (SGOT)/ALT (SGPT): 0.8-1.5;
  • Serum creatinine: 41-81 μmol/L;
  • Other situations where the researcher thinks it is inappropriate to participate in this research.

研究组 & 干预措施

Limonene capsules(marketed product in China)

Active Comparator

Limonene capsules(marketed product in China) donate by pharmaceutical company.

干预措施: Limonene capsule (Drug)

Limonene capsules(Placebo)

Placebo Comparator

Same smell, color and shape as limonene capsules(marketed product in China), without limonene in capsules.

干预措施: Limonene capsules(Placebo) (Drug)

结局指标

主要结局

Changes in the sum of longest diameters of target nodules (multiple nodules) between the drug group and the placebo group.

时间窗: at baseline, three months and six months after administration

Difference in the sum of longest diameters of target nodules

次要结局

  • Overall response rate of participants as measured by RECIST criteria between the two groups(at baseline, three months and six months after administration)
  • Changes in the sum of longest diameters of baseline target nodules (multiple nodules) between the drug group and the placebo group(at baseline and twelve months after administration)
  • Change in density of baseline target nodules between the two groups.(at baseline, three months and six months after administration)
  • Change in density of baseline non-target nodules between the two groups(at baseline, three months and six months after administration)
  • Adverse events(at baseline, three months and six months after administration)
  • Cytokine detection(at baseline, three months and six months after administration)
  • Change in diameters of baseline target nodules (single nodule) detected by CT between the two groups.(at baseline, three months and six months after administration)
  • Change in the longest diameters size of baseline non-target nodules between the two groups(at baseline, three months and six months after administration)
  • Change in numbers of baseline non-target nodules between the two groups(at baseline, three months and six months after administration)
  • Value of serum miRNA(at baseline, three months and six months after administration)
  • Plasma metabolomics(at baseline, three months and six months after administration)
  • Proportion of circulating blood immune cells(at baseline, three months and six months after administration)

研究者

发起方
Shanghai Jiao Tong University School of Medicine
申办方类型
Other
责任方
Principal Investigator
主要研究者

Biyun Qian

Professor

Shanghai Jiao Tong University School of Medicine

研究点 (1)

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