- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT01697683
Probiotic Therapy for the Reversal of Bacterial Vaginosis in Pregnancy (ProVIP)
20 mars 2014 uppdaterad av: Mount Sinai Hospital, Canada
This study will add to the current knowledge and literature on the ability of an oral lactobacilli preparation to return the vaginal flora to a normal state in pregnant women.
The results will potentially serve as the basis for a multi-centre Phase III randomized clinical trial to determine the efficacy of this treatment in preventing preterm birth.
Studieöversikt
Status
Avslutad
Intervention / Behandling
Detaljerad beskrivning
Preterm birth continues to provide the greatest challenge in perinatal health care in the developed world.
It is a syndrome involving multiple causes and arises from a number of social, psychological, and biological determinants.
It has been estimated that intrauterine infection accounts for at least 25-40% of spontaneous preterm births, with infection being the primary cause of extreme prematurity.
Because infection-mediated preterm delivery mainly occurs in younger gestational ages (less than 28 weeks), these extremely premature babies not only have the risks associated with being born early, but are also likely to have severe morbidities associated with infection.
Bacterial vaginosis (BV) is defined as a loss or significant depletion of lactobacilli coupled with an overgrowth of pathogenic bacteria and an increase in vaginal pH (>4.5).
BV is common and occurs in 20% of the general female population, often without symptoms and is associated with a 40% increased risk of preterm birth.
The clinical finding that lactobacilli is the dominant microbe in the vagina of women with a healthy pregnancy and full term delivery, supports the association of this species with a healthy pregnancy.
BV is associated with an elevation of cervico-vaginal pro-inflammatory cytokines including IL-1β and IL-8 that are also associated with preterm labour; initiating the inflammatory cascade of events involved in labour may be the mechanism by which BV triggers preterm birth.
However, not all women with BV will deliver preterm suggesting that variations in genetic susceptibility may underlie the host response to the presence of BV and the risk for preterm birth.
Antibiotic therapy is the current treatment for BV, but the extent to which antibiotics can prevent preterm birth in women with BV remains somewhat uncertain, with conflicting results published in the literature.
The apparent ineffective nature of antibiotic therapy, perhaps due to a lack of regrowth of lactobacilli following treatment, and the possibility that the pathogens have already induced inflammatory processes that will eventually induce preterm birth, emphasizes the need to continue to investigate the role of microbes during pregnancy.
Probiotics have been suggested as an alternative to antibiotic therapy in restoring vaginal lactobacilli and reversing BV.
The study seeks to determine whether Lactobacillus rhamnosus, GR-1 and Lactobacillus reuteri, RC-14 when administered to pregnant women diagnosed with bacterial vaginosis or intermediate flora will reverse the condition leading to a decrease in the inflammatory mediators involved in the cascade of infection/inflammation-mediated preterm birth.
Studietyp
Interventionell
Inskrivning (Faktisk)
86
Fas
- Fas 2
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
-
-
Ontario
-
Toronto, Ontario, Kanada, M5G 1X5
- Mount Sinai Hospital
-
-
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
18 år till 50 år (Vuxen)
Tar emot friska volontärer
Ja
Kön som är behöriga för studier
Kvinna
Beskrivning
Inclusion Criteria:
- pregnant women prior to 17 weeks gestation
- singleton pregnancy
- over 18 years of age
- able to provide informed consent
Exclusion Criteria:
- multifetal pregnancies (twins, triplets, etc)
- fetal complications (congenital anomaly, chromosomal abnormality)
- maternal history of previous preterm birth or second trimester loss
- significant maternal medical or surgical complications (eg. hypertension, diabetes)
- less than 18 years of age
- unable to provide informed consent
- HIV Positive
- Immuno-compromised
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Fyrdubbla
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Placebo-jämförare: Sockerpiller
|
|
|
Aktiv komparator: Probiotic Rhamnosus Lactobacilli
|
Two capsules per day containing either probiotic lactobacilli or placebo for 12 weeks
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Microbial DNA profile
Tidsram: At 28 and at 35 weeks gestation
|
A change in the Vaginal Microbial DNA profile
|
At 28 and at 35 weeks gestation
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Microbial function
Tidsram: At 28 and at 35 weeks gestation
|
A change in microbial function as measured by RNA transcriptomics
|
At 28 and at 35 weeks gestation
|
Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Sponsor
Samarbetspartners
Utredare
- Huvudutredare: Alan Bocking, MD, Mount Sinai Hospital
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart
1 maj 2012
Primärt slutförande (Faktisk)
1 mars 2014
Avslutad studie (Faktisk)
1 mars 2014
Studieregistreringsdatum
Först inskickad
28 september 2012
Först inskickad som uppfyllde QC-kriterierna
1 oktober 2012
Första postat (Uppskatta)
2 oktober 2012
Uppdateringar av studier
Senaste uppdatering publicerad (Uppskatta)
24 mars 2014
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
20 mars 2014
Senast verifierad
1 mars 2014
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- 08-0005-A
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .