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Clinical Trials/NCT02692820
NCT02692820CompletedNot Applicable

Preventing Preterm Birth With Probiotics - Pilot Randomised Trial

Queen Mary University of London2 sites in 1 country304 target enrollmentStarted: May 1, 2016Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
304
Locations
2
Primary Endpoint
The microbiological effect of the probiotic on the vaginal flora during pregnancy,

Study Overview

Brief Summary

Babies born preterm (before completing 37 weeks in the womb) are at increased risk of long-term disability and death. The investigators do not fully understand the cause(s) of preterm birth but it occurs more frequently when the normal, healthy bacteria (called Lactobacilli) in a woman's birth canal are replaced with unhealthy bacteria. Previous attempts to get rid of the unhealthy bacteria with antibiotics have not shown to affect the risk of preterm birth. The reason for this may be that what is required is the replacement of Lactobacilli in the birth canal. This can be done by asking women to take capsules containing lactobacilli once daily. To study whether oral Lactobacilli capsules compared with dummy capsules can reduce the risk of preterm birth, a large study involving approximately 10,000 women would be required. But the investigators do not know whether women would agree to take part in and complete such a study, and this is what the investigators wish to study in the small, initial study described here. The results of this study will show whether probiotics produce the desired biological effects on vaginal bacteria, and whether it would be feasible to perform the larger, definitive study of their effectiveness in prevention of preterm birth.

Detailed Description

Preterm birth (PTB) is defined as the birth of a baby before the completion of 37 weeks gestation in the womb. It is the major cause of infant mortality particularly during the first month of life. Approximately 75 per cent of babies who die during the first 28 days of life are born before 37 weeks gestation. Survivors of PTB are at increased risk of long-term disabilities such as cerebral palsy, sight and hearing impairment, learning and behavioural problems, epilepsy, and hospital readmissions. Even late preterm births, defined as PTB at 34--36 weeks gestation, which account for 70% of all preterm births in England and Wales, are at increased risk of death and disability compared with babies born at term. Although the prevalence of adverse long--term outcome is highest among children born at the earliest gestational ages, the much higher number of births at 34--36 weeks of gestation compared with earlier gestations means that this group of children makes a major contribution to the number of children adversely affected. PTB and its consequences can have negative emotional and psychosocial impacts on parents and families.

In addition to its impact on individuals and families, the financial consequences for the public sector of caring for children born preterm are significant. The cost of care up to the age of 18 for children born preterm has been estimated to exceed £3 billion per year in England and Wales at 2006 prices. It has been estimated that a hypothetical intervention that delayed PTB by 1 week across all gestational age categories would reduce the public sector cost of PTB by £1 billion annually.

About one third of PTBs occur because early delivery is indicated due to complications in the mother or the unborn baby (fetus); the remaining two thirds occur spontaneously. The rate of PTB has increased by 19% from 1990 to 2010 in developed countries. At the same time, there has been a marked improvement in the survival rates of PTBs but a similar reduction in adverse outcomes has not been seen. Thus, the absolute numbers of individuals adversely affected is increasing.

Infection within the womb (intrauterine infection) is strongly associated with spontaneous PTB. The commonest pathway for intrauterine infection is the ascent of unhealthy bacteria from the vagina and cervix into the womb. Bacterial vaginosis (BV), in which the normally dominant healthy bacteria in the vagina (lactobacilli) are replaced with unhealthy bacteria, is strongly associated with PTB. Lactobacilli, principally the strains that produce higher levels of the chemical hydrogen peroxide, appear to protect against BV and reduce the risk of PTB.

Despite substantial evidence linking BV with PTB, the results of trials of antibiotic treatment of BV in pregnancy have not produced clear evidence of benefit. The reason for this might be that it is not the eradication of unhealthy bacteria that is required but rather the replacement of unhealthy bacteria with the normally dominant lactobacilli. One way of achieving this could be by administering lactobacilli-containing capsules (probiotics) to pregnant women. Oral probiotics taken during pregnancy may directly alter the vaginal bacteria and in so doing protect the cervical opening from ascending infection.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
16 Years to — (Child, Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Women aged 16 years and over at the time of the booking appointment.
  • •Women who are between 9-14 weeks gestation at the time of the dating scan.

Exclusion Criteria

  • •Lack of informed, written consent

Arms & Interventions

Placebo

Placebo Comparator

Those who provide consent will be randomised to receive once daily for the remainder of their pregnancy capsules of the placebo containing excipients alone in a gelatin capsule

Intervention: Placebo Comparator (Other)

Probiotic

Experimental

Those who provide consent will be randomised to receive once daily for the remainder of their pregnancy capsules of probiotics (containing Lactobacillus rhamnosus GR-1 and Lactobacillus reuteri RC-14 (each at 2.5 x 109 colony forming units (CFUs)). The product contains freeze-dried bacteria and excipients in a gelatin capsule.

Intervention: Probiotic (Dietary Supplement)

Outcomes

Primary Outcomes

The microbiological effect of the probiotic on the vaginal flora during pregnancy,

Time Frame: 18 months

To evaluate the microbiological effects of probiotics on vaginal flora the investigators will compare treatments groups regarding the proportion of women with bacterial vaginosis (BV) at delivery and the proportion of women with vaginal colonisation with intervention strains at delivery.

The proportion of eligible women recruited into the trial

Time Frame: 18 months

The primary analysis will also involve the estimation of the proportions of the primary outcomes (i.e. eligible women recruited into the trial, recruited women who complete the trial and adhere to the intervention treatment until delivery).

The proportions of recruited women who complete the trial and adhere to the intervention until delivery

Time Frame: 18 months

The primary analysis will also involve the estimation of the proportions of the primary outcomes (i.e. eligible women recruited into the trial, recruited women who complete the trial and adhere to the intervention treatment until delivery).

Secondary Outcomes

  • Questionnaire/interview assessment of reasons for participation and non-participation, trial attrition, and non-adherence to trial protocol by ethnic groups (subject to funding)(18 months)
  • Core outcomes for use in studies on preterm birth prevention from case report forms(18 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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