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临床试验/NCT03671486
NCT03671486已完成不适用

Observational Study to Investigate the Probability of Colonization with Group B Streptococcus (GBS) of Pregnant Women Who Were Negative for GBS in the First Trimester of Pregnancy

ProbiSearch SL1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2018年12月5日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
100
试验地点
1
主要终点
Participants (%) with a vaginal-rectal detection of Group B Streptococcus.

研究概览

简要总结

An observational study to estimate the probability of pregnant women, who were GBS-negative in the first trimester of pregnancy become GBS-positive at the end of pregnancy. It is an observational. One hundred pregnant women in the first trimester of pregnancy (11 ± 2 weeks) will be invite to participate in this prospective study. If accept, a vagino-rectal swab will collected for a GBS detection analysis. When negative, participants will be follow by their gynecologist with the normal routine procedures. During 35 week of pregnancy a vagino-rectal swab will be collected and analyzed to detect GBS. Then, a final visit will be completed one month after delivery.

详细描述

Healthy pregnant women reporting to the clinic in their first trimester of pregnancy (week 11 ± 2 weeks of pregnancy) will be asked to participate in this study. Participation will be voluntary and written informed consent will be obtained from each participant. The study visits will take place in the hospital.

At Visit 1, the inclusion and exclusion criteria will be verified. After signing the informed consent, a physical examination will be performed in addition to a vaginal-rectal swab to detect if they are GBS-negative. Information on the demographic profile and medical history will be collected. The investigator will explain to the participant that she cannot use any probiotic during the course of the study.

At Visit 2, within 21-23 weeks ± 4 days of gestation, the inclusion and exclusion criteria will be reviewed. If the result of the microbiological analysis of the vaginal-rectal exudate is negative, the pregnant women shall continue in the study. A physical examination will be performed. Adverse Events occurring from the time of study inclusion will be recorded.

At the third visit (Visit 3, 35 weeks ± 4 days of gestation), all participants continuing in the study will undergo a general physical examination. A sample of vagino-rectal exudate will be collected. Adverse Events occurring during the period between Visit 2 and Visit 3 will be recorded.

During Visit 4 (1 month after delivery), all participants will have a general physical examination. Adverse Events occurring since Visit 3 will be recorded. Data will be collected on the delivery and occurrence of early- or late-onset GBS sepsis in the newborn during the first month of life.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • Healthy pregnant women, adults (≥ 18 years and under 45 years). Before/during week 13 of gestation. Signing of informed consent.

排除标准

  • Multiple pregnancy.
  • Fetal complications.
  • History of premature delivery/miscarriage in the second trimester. Significant maternal medical complications.
  • HIV-positive.
  • Women who are immunocompromised (for example, patients with cancer and transplant who are taking certain immunosuppressive drugs, patients with hereditary diseases that affect or could affect the immune system).
  • History of significant gastrointestinal disease (e.g., prior gastrointestinal resection, current diarrhea, inflammatory bowel disease).
  • Heart failure and cardiac medical history (e.g. artificial heart valve, medical history of infective endocarditis, rheumatic fever or cardiac malformation).
  • Use of other probiotics during the current pregnancy.
  • Uncertainty of the investigator regarding the willingness or capacity of the participant to comply with the requirements of the protocol.

结局指标

主要结局

Participants (%) with a vaginal-rectal detection of Group B Streptococcus.

时间窗: 6 months

Percentage of participants with a vaginal-rectal detection of Group B Streptococcus at the end of the study.

次要结局

  • Premature detachment of the placenta(7 months)
  • Pregnancy complications(7 months)
  • Premature delivery(7 months)
  • Newborns with early onset sepsis(7 months)
  • Newborns with late onset sepsis(7 months)
  • Composition of the microbiota of vaginal-rectal exudates(6 months)
  • Premature membrane rupture(7 months)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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