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CompletedNCT03303859VaMapUpdated May 30, 2018

Bacterial Vaginosis Carriage in Early Pregnancy and Preterm Delivery in Martinique, F.W.I

An observational study in Bacterial Vaginosis, sponsored by University Hospital Center of Martinique. Completed. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2018-05-30.

Sponsored by University Hospital Center of Martinique · Observational

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Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
511
Ages
18 Years and older
Sex
Female
01

Study summary

Preterm delivery is a public health priority in Martinique, a French oversees territory located in the Caribbean, with a rate of 10,5% substantially higher than in Continental France (7,5%). Bacterial vaginosis is an imbalance of vaginal flora known to be associated with preterm delivery risk. Studies driven in the United States have pointed out that 50% of the excess in preterm birth rate observed in Afro-American population compared to Caucasian population may be attributable to infection. Bacterial vaginosis appears much more prevalent in our population than in Continental France (approximatively 30% versus 7%) and may constitute an explanation to the discrepancy in preterm delivery rate.

Read the detailed description

Bacterial vaginosis during pregnancy is considered as a risk factor for preterm birth since the 1990's. A meta-analysis realized in 2003 found an Odds ratio of 2.4 for preterm delivery among women with bacterial vaginosis carriage, culminating at 7.5 when carriage before 17 weeks gestation was considered. Preterm delivery is a pregnancy complication known to be more prevalent among patients of African descent. Various hypothesis have been tested to account for this observed discrepancy and several authors consider that up to 50% of the difference in preterm delivery rate between Afro-american and Caucasians may have and infectious origin, with up to 30% attributable to a very different bacterial vaginosis carriage among patients of various ethnic origin. Several factors may interfere in the link observed between bacterial vaginosis and preterm delivery, which are also unevenly distributed among women of different ethnic origin. Exposure to stress, low socio-economic status, single marital status or low access to prenatal care are among those factors. Thus analyzing a relation between bacterial vaginosis and preterm delivery mandates to control for such factors. The present study will proceed to a vaginal sampling before 17 gestational age (GA) to diagnose a bacterial vaginosis through the Nugent score which is the standard diagnostic method for this pathology. At the same time, a written survey concerning stressful events in the past 12 months is submitted to volunteer patients in order to use the social readjustment rating scale by Holmes and Rahe and to account for the role of stress as a potential confounding factor. Socio-demographic data, obstetrical history and complications during pregnancy were also recorded and patients followed-up prospectively until delivery. Caregivers were blinded to the results of initial vaginal sampling. No alteration of the normal pregnancy follow-up was required by the study design.

02

Conditions studied

  • Bacterial Vaginosis

Keywords

  • Bacterial vaginosis, preterm delivery, Martinique, stress
03

In context

Vaginosis, Bacterial

240 studies on the registry are indexed under Vaginosis, Bacterial; 39 are open to participants now.

This study's enrollment of 511 is above the median of 350 across 30 observational studies indexed under Vaginosis, Bacterial.

Browse Vaginosis, Bacterial studies →

Lead sponsor

University Hospital Center of Martinique is the lead sponsor of 79 studies on the registry; 21 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Sampling method
Non-probability sample

Study population

Bacterial vaginosis appears much more prevalent in Martinique than in Continental France (approximatively 30% versus 7%) and may constitute an explanation to the discrepancy in preterm delivery rate.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • All women followed-up since the beginning of pregnancy in the study center and supposed to deliver in this same center

Exclusion criteria

Exclusion Criteria:

  • Previous preterm delivery,
  • Previous late abortion,
  • Multiple pregnancy,
  • Cervical cerclage before inclusion
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
511 participants (actual)
Patient registry
No

Interventions

  • Diagnostic testBacterial vaginosis
06

What researchers measure

Primary outcomes

  1. Preterm delivery before 37 weeks gestation

    Rate of preterm delivery

    Time frame: 37 weeks gestation

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Dec 2013 to primary completion in Jun 2016, 30 months.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 3, 2017
First posted
Oct 6, 2017
StartActual
Dec 18, 2013
Primary completionActual
Jun 26, 2016
CompletionActual
Jun 23, 2017
Last update
May 30, 2018
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on May 30, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03303859
Lead sponsor
University Hospital Center of Martinique
Responsible party
Sponsor
First posted
Oct 6, 2017
Start date
Dec 18, 2013
Primary completion
Jun 26, 2016
Completion
Jun 23, 2017
Last update
May 30, 2018

Study contacts

Jean-Luc VOLUMENIE
principal investigator · CHU de Martinique

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2018. You cannot join it, but the record below documents what was studied.

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