- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT01697683
Probiotic Therapy for the Reversal of Bacterial Vaginosis in Pregnancy (ProVIP)
20. mars 2014 oppdatert 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.
Studieoversikt
Status
Fullført
Intervensjon / Behandling
Detaljert beskrivelse
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.
Studietype
Intervensjonell
Registrering (Faktiske)
86
Fase
- Fase 2
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
-
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Ontario
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Toronto, Ontario, Canada, M5G 1X5
- Mount Sinai Hospital
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-
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
18 år til 50 år (Voksen)
Tar imot friske frivillige
Ja
Kjønn som er kvalifisert for studier
Hunn
Beskrivelse
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
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Firemannsrom
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Placebo komparator: Sukkerpille
|
|
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Aktiv komparator: Probiotic Rhamnosus Lactobacilli
|
Two capsules per day containing either probiotic lactobacilli or placebo for 12 weeks
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Microbial DNA profile
Tidsramme: At 28 and at 35 weeks gestation
|
A change in the Vaginal Microbial DNA profile
|
At 28 and at 35 weeks gestation
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Microbial function
Tidsramme: At 28 and at 35 weeks gestation
|
A change in microbial function as measured by RNA transcriptomics
|
At 28 and at 35 weeks gestation
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Samarbeidspartnere
Etterforskere
- Hovedetterforsker: Alan Bocking, MD, Mount Sinai Hospital
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart
1. mai 2012
Primær fullføring (Faktiske)
1. mars 2014
Studiet fullført (Faktiske)
1. mars 2014
Datoer for studieregistrering
Først innsendt
28. september 2012
Først innsendt som oppfylte QC-kriteriene
1. oktober 2012
Først lagt ut (Anslag)
2. oktober 2012
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
24. mars 2014
Siste oppdatering sendt inn som oppfylte QC-kriteriene
20. mars 2014
Sist bekreftet
1. mars 2014
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 08-0005-A
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .