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临床试验/NCT07295314
NCT07295314尚未招募1 期

Effect of Antifungals on the Intestinal Microbiome - a Randomized, Controlled, Proof-of-concept Trial

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2026年1月1日最近更新:
干预措施

试验速览

阶段
1 期
状态
尚未招募
入组人数
50
试验地点
1
主要终点
Effect of fluconazole on the intestinal microbiome

研究概览

简要总结

The goal of this clinical trial is to learn how the antifungal drug fluconazole affects the gut microbiome and immune system in healthy volunteers.

The main questions it aims to answer are:

  • Does fluconazole change the gut bacteriome and mycobiome composition after 14 days of treatment?
  • How long do these changes last (4 weeks and 6 months after treatment)?
  • Does fluconazole affect the body's immune responses, such as blood cell activity and antifungal antibodies?

Researchers will compare two groups: participants who take fluconazole for 14 days and participants who receive no intervention.

Participants will:

  • Either take one fluconazole tablet (200 mg) daily for 14 days, or receive no treatment
  • Provide stool samples and blood samples at several timepoints
  • Return for follow-up visits up to 6 months after treatment

This study is conducted at Amsterdam UMC, location AMC, with a planned enrollment of 50 healthy male volunteers aged 18-35 years.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • Male, 18-35 years of age at the time of signing informed consent
  • Healthy, as determined by medical history and physical examination; minor clinical abnormalities allowed if not introducing additional risk or interfering with study procedures
  • Capable of giving written informed consent and able to comply with study requirements
  • Normal defecation pattern (≤3 times/day and ≥3 times/week)

排除标准

  • Major illness in the past 3 months, or significant chronic medical illness deemed unfavorable for enrollment
  • Past or current gastrointestinal disease that may influence the gut microbiota (including inflammatory bowel disease or medication-treated irritable bowel syndrome)
  • History of immunodeficiency
  • History of malignancy
  • Alcohol intake >3 units/day on average
  • Known allergy to antifungal drugs
  • Use of antibiotics (except topical) within the past 3 months
  • Use of antifungals (except topical) within the past 3 months
  • Planned prolonged travel (>4 weeks) to tropical countries during the study period
  • Receipt of an investigational product within 3 months prior to study day 0
  • Use of prescription or non-prescription drugs, herbal or dietary supplements within 3 months (unless deemed safe by investigator)
  • Difficulty with blood donation or poor venous access in either arm
  • Donation of >500 mL of blood in the past 3 months
  • Any other condition or circumstance that, in the investigator's opinion, could be harmful to the subject or compromise data interpretation

研究组 & 干预措施

Fluconazole

Experimental

Participants will receive oral fluconazole 200mg once daily for 14 days.

干预措施: Fluconazole 200mg tab (Drug)

结局指标

主要结局

Effect of fluconazole on the intestinal microbiome

时间窗: 14 days (end of treatment)

Difference in gut bacteriome and mycobiome composition, ⍺- and ß-diversity between adults treated with an antifungal (fluconazole) and no intervention directly after completion of antifungal treatment (t=14 days).

次要结局

  • Gut microbiome and mycobiome composition at 6 months post-treatment(6 months post-treatment)
  • Gut microbial functional profiles after fluconazole treatment(Baseline, 14 days, 4 weeks, and 6 months)
  • Systemic innate immune responses after fluconazole treatment(Baseline, 14 days, 4 weeks, and 6 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

W. J. Wiersinga, MD

Professor

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

研究点 (1)

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