Preterm birth (PTB) is the primary cause of infant death worldwide. It has been shown that a vaginal microbiota deplete in Lactobacillus species is a risk factor for preterm labour. Conversely a vaginal microbiota dominated by Lactobacillus crispatus appears to be protective for these adverse outcomes. A wide range of 'over the counter' Lactobacillus spp. containing products targeted at 'vaginal health' and formulated for vaginal administration are available, but most of them do not contain vaginal species of Lactobacillus. The primary aim of this study is to determine whether vaginal supplementation with L. crispatus CTV-05 is associated with colonisation.
Pregnant women at Queen Charlotte's and Chelsea Hospital and St Mary's Hospital London who are defined as being at a higher than background risk for preterm labour will be recruited into this study. Women at risk of pre-term labour will include those with either previous LLETZ, previous preterm birth, previous second trimester pregnancy loss or a combination of these indications. As part of this interventional study, subjects will be offered supplementation with L. crispatus CTV-05. The preparation of LACTIN-V is administered vaginally using a specially designed applicator. The primary aim of this study is to determine whether vaginal supplementation with L. crispatus CTV-05 is associated with colonisation.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
PREVENTION
Masking
NONE
Enrollment
60
Vaginal supplementation with L. crispatus CTV-05.
Institute of Reproductive Developmental Biology, Hammersmith Hospital
London, United Kingdom
RECRUITINGThe number of participants that demonstrate a change in vaginal colonisation during and following LACTIN-V use.
Microbiological effects of LACTIN-V by laboratory analysis, next generation sequencing
Time frame: 2-4 years
The number of participants with treatment related adverse events following LACTIN-V supplementation in pregnant women at high risk of preterm birth.
Participants will be asked about adverse events during clinical review and the safety profile will be recorded.
Time frame: 2-4 years
The number of patients using LACTIN-V that go on to experience preterm birth, PPROM or cervical shortening.
Clinical outcomes of participants will be analysed, in accordance with colonisation results
Time frame: 2-4 years
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