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临床试验/NCT04517487
NCT04517487进行中(未招募)1 期

Vaginal Microbiome Transplantation for Recurrent Bacterial Vaginosis-A Placebo, Randomized, Controlled Trial

Hadassah Medical Organization2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2020年8月20日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
30
试验地点
2
主要终点
Microbiome composition

研究概览

简要总结

Vaginal Microbiome Transplantation (VMT) may be beneficial in treating the most severe cases of recurrent and antibiotics-nonresponsive cases of BV. Recently, we completed a preliminary study in which we treated patients with recurrent and antibiotics-non-responsive, intractable BV, with VMT from healthy donors [Lev-Sagie, Nature Medicine 2019]. Four VMT recipients in this preliminary study featured a significant improvement of both clinical symptoms and dysbiotic vaginal microbiome composition and function, which persisted over a long follow-up period, while one recipient featured a partial remission.

The proposed study is designed as a placebo, randomized controlled trial, and is aimed to further assess whether VMT may serve as a viable option in symptomatic, intractable BV. In the suggested study, we plan to compare transplantation of: 1) vaginal fluid from healthy donors, and 2) saline (placebo).

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Ages 18-50
  • Recurrent BV, defined as ≥4 symptomatic episodes of BV during the last year, who require maintenance antibiotic treatment (twice weekly) in order to remain symptom-free, or if they experienced recurrence of BV in ≤ 2 months following antibiotic treatment, with a documented history of recurrent BV in the last year.
  • Patients are otherwise healthy.
  • Contraception use

排除标准

  • Pregnancy or a planned pregnancy in the upcoming year
  • Infection with HIV.
  • Immunodeficiency status.

研究组 & 干预措施

VMT recipients

Active Comparator

In order to prevent transfer of pathogens, sperm, or antibiotic-resistant commensals we will establish a "vaginal fluid bank" in which samples from suitable donors will be kept for future use:

  • Donors will be screened using a questionnaire addressing risk factors for potentially transmissible infections, undergo screening for cervico-vaginal infections, cervical cytology screening, and serology analysis for transmittable infections {see detailed screening in Lev-Sagie et al. Nat Med. 2019;25(10):1500-1504. doi: 10.1038/s41591-019-0600-6.}
  • The collected samples for VMT will be examined for bacteria,viruses and sperm.

Before transplantation, patients will be treated with intravaginal antibiotics. A frozen specimen will be thawed at room temperature and will be placed in the patient's vagina.

Following VMT, patients will be evaluated every 14 days for the first month, then every month for additional 11 months.

干预措施: Vaginal Microbiome Transplantation (VMT) (Biological)

Placebo

Placebo Comparator

Saline with glycerol will be used as placebo. Before transplantation, patients will be treated with intravaginal antibiotic.

Following Placebo, patients will be evaluated every 14 days for the first months, then every month for additional 2-4 months.

After 4 months, patients who initially received placebo will be offered a VMT in case they are still symptomatic and fulfill inclusion criteria, in an open-label phase.

干预措施: Placebo (Biological)

结局指标

主要结局

Microbiome composition

时间窗: 12 months

Characterization of the vaginal microbial community using shotgun analysis and16S rRNA sequencing

Laboratory parameters- Amsel criteria

时间窗: 12 months

Presence or absence of each Amsel criteria (discharge, pH\>4.5, positive whiff test and clue cells on microscopy)/

Vaginal fluid microscopy

时间窗: 12 months

Presence of Lactobacillus-dominant microbiome on microscopy

Clinical parameters- patient's complains

时间窗: 12 months

Number of participants reporting disappearance of discharge and odor

Clinical parameters- patient's complains

时间窗: Interim analysis at 4 months from initail intrvention, and final analysis at 12 months.

Number of participants reporting disappearance of discharge and odor

Laboratory parameters- Amsel criteria

时间窗: Interim analysis at 4 months from initail intrvention, and final analysis at 12 months.

Presence or absence of each Amsel criteria (discharge, pH\>4.5, positive whiff test and clue cells on microscopy)/

Vaginal fluid microscopy

时间窗: Interim analysis at 4 months from initail intrvention, and final analysis at 12 months.

Presence of Lactobacillus-dominant microbiome on microscopy

Microbiome composition

时间窗: Interim analysis at 4 months from initail intrvention, and final analysis at 12 months.

Characterization of the vaginal microbial community using shotgun analysis and16S rRNA sequencing

次要结局

未报告次要终点

研究者

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

Ahinoam Lev-Sagie

Principal investigator

Hadassah Medical Organization

研究点 (2)

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