drugset / Trial / NCT06349122

Screen-and-treat Strategy for Vaginal Flora Abnormalities in Pregnant Women at High Risk of Preterm Birth

NCT06349122

Phase 4 Not yet recruiting 1292 enrolled Assistance Publique Hopitaux De Marseille
RandomizedParallel-groupOpen-labelTreatment

Summary

Preterm birth is an important cause of death and disabilities. Bacterial vaginosis (BV) is a common vaginal dysbiosis or abnormal microbiota, with a predominance of anaerobic bacteria with a lack of Lactobacillus, with various diagnosis methods. Often asymptomatic, BV increases the risk of preterm birth according to the gestational age at diagnosis. BV is usually diagnosed by conventional diagnosis such as Nugent score. Molecular diagnosis of BV has been demonstrated to be more reproducible, more accurate and to better define dysbiosis. The main objective of the study is to evaluate the effectiveness of an innovative screen-and-treat strategy for vaginal flora abnormalities by molecular biology using a Point of Care multiplex technology before 18 weeks' gestation to reduce the rate of preterm birth in a population of pregnant women at high risk of preterm birth. The hypothesis is that a strategy for screening and treating vaginal flora abnormalities and their recurrences using molecular biology in women with a history of prematurity or late-term abortion could be effective in reducing premature births by 40%.

Timeline

Start
2024-08
Primary completion
2027-03
Completion
2028-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Azithromycin Small molecule 1 g Oral
Subject Azithromycin Small molecule 2 g Oral
Subject Ceftriaxone Other / unclassified 1 g Intramuscular
Subject Clotrimazole Unknown Other
Subject Metronidazole Small molecule 2 g Other

Indications