Effect of Probiotics on the Preterm Delivery Rate in Pregnant Women at High Risk for Preterm Birth

NCT ID: NCT03689166

Last Updated: 2022-09-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

200 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-10-23

Study Completion Date

2022-06-16

Brief Summary

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Preterm birth (PB) continues to be the main cause of perinatal morbidity and mortality, with emotional and economic consequences. Despite improvements in health, PB prevalence remains stable, possibly due to complex causes such as maternal age, stress, multiparity, etc. Shortening of the uterine cervix in early stages of gestation is a risk factor for PB. The presence of abnormal vaginal microbiota in the early stages of pregnancy is als a risk factor for PB. However, no studies have analysed the impact of probiotics (live microorganisms which, in adequate amounts, confer a health benefit on the host) on the PB in high-risk PB patients (pregnant women with threatened preterm delivery, i.e., uterine contractions and cervical shortening, with a 30% PB risk before 34 weeks, and 50% PB prior to 37 weeks (\> 6-10% PB). Similarly, the effect of probiotics on vaginal flora dominated by lactic acid-producing bacteria could be analysed.

Detailed Description

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Hypothesis

* Pregnant women with threatened preterm labour (TPL) will present vaginal microbiome different from those without TPL.
* Treatment with probiotics will modify the vaginal microbioma of pregnant women with TPL.
* The PB rate before 37 weeks in pregnant women with TPL who have received probiotics since their diagnosis will be reduced by at least 30%.

Goals

* To correlate the use of probiotics of pregnant women with TPL with the PB rate before 37 weeks.
* To ascertain the PB rate before 28, 30, 32 and 34 weeks in both groups.
* To assess neonatal morbidity between both groups.

Methods

Prospective, randomised, longitudinal, prospective, double-blind study.

Relevance

This study will determine whether the use of probiotics in pregnant women with TPL is associated with a lower risk of PB before 37 weeks. If so, it would allow us to act on the tertiary prevention of PB and treatment of TPL, the main cause of perinatal morbidity and mortality in our setting. It will also facilitate understanding of the pathophysiology of PB, influence of vaginal microbiota and the mechanism of action of probiotics.

Conditions

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Preterm Birth

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Definition and design. Prospective, double-blind randomised study.

Population Pregnant women admitted for TPL between weeks 24.0 and 34.6 of gestation at the participating centre.
Primary Study Purpose

TREATMENT

Blinding Strategy

QUADRUPLE

Participants Caregivers Investigators Outcome Assessors
Double-blinded RCT

Study Groups

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Probiotics group

Probiotic drug

Group Type ACTIVE_COMPARATOR

Probiotic

Intervention Type DIETARY_SUPPLEMENT

Reduce preterm birth with this dietary supplement

Control group

This group will receive placebo

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type OTHER

Placebo

Interventions

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Probiotic

Reduce preterm birth with this dietary supplement

Intervention Type DIETARY_SUPPLEMENT

Placebo

Placebo

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Threatened preterm labour: regular clinical and cardiotography-registered uterine dynamics, and cervical modifications (cervical shortening ≤ 25 mm between 24 and 29 weeks, and ≤ 15 mm between 30 and 34 weeks) according to our care protocol.
* Single gestation.
* Echographically-normal foetal morphology.
* Minimum age 18 years.
* Ability to understand informed consent.
* Signed informed consent.

Exclusion Criteria

* Multiple gestations.
* Pregnant women with diagnosis of chorioamnionitis.
* Cervical dilation.
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Maternal-Infantil Vall d´Hebron Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Hospital Vall d'Herbron

Barcelona, , Spain

Site Status

Countries

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Spain

References

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Del Barco E, Molano LG, Vargas M, Miserachs M, Puerto L, Garrido-Gimenez C, Soler Z, Munoz B, Pratcorona L, Rimbaut S, Vidal M, Dalmau M, Casellas A, Carreras E, Manichanh C, Goya M. The Effect of Probiotics on Preterm Birth Rates in Pregnant Women After a Threatened Preterm Birth Episode (The PROPEV Trial). Biomedicines. 2025 May 8;13(5):1141. doi: 10.3390/biomedicines13051141.

Reference Type DERIVED
PMID: 40426968 (View on PubMed)

Other Identifiers

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PR(AMI)236/2016

Identifier Type: -

Identifier Source: org_study_id

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