Premature Delivery

2

Review clinical trials related to Premature Delivery. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Effect of Intelligent Intervention Strategies on Self-efficacy and Hospital Readiness of Parents of Preterm Infants

1. Construct intelligent management intervention plan for parents of preterm infants from hospital to family based on the medical and health system suitable for China's national conditions. 2. Clinical randomized controlled trials were conducted to verify and evaluate the feasibility and application effect of the intervention program.

Participants needed: 84
Trial details
Age: 18-100Biological sex: AllType: InterventionalSponsor: Shantou University Medical CollegeUpdated: Oct 10, 2024
Eligibility criteria

Inclusion criteria for premature infants ① gestational age < 37 weeks;② Prema... [+1]

Exclusion criteria for preterm infants ① intrauterine developmental retardation... [+1]

Status: Not yet recruiting

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

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%.

Participants needed: 1,292
Trial details
Phase: Phase 4Age: 18+Biological sex: FemaleType: InterventionalSponsor: Assistance Publique Hopitaux De MarseilleUpdated: Apr 5, 2024
Eligibility criteria

Pregnant women over 18 years of age [+4]

- Woman of legal age under legal protection; [+12]