Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06849037

Comparing Infectious Morbidity Among Women With Meconium-stained Amniotic Fluid at Term, Between Those Treated With Prophylactic Antibiotics Zinacef vs. Placebo

and Infectious Morbidity Among Women With Meconium-stained Amniotic Fluid at Term, Between Those Who Will be Treated With Prophylactic Antibiotics Zinacef vs. Placebo

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
182 (estimated)
Sponsor
Western Galilee Hospital-Nahariya · Other Government
Sex
Female
Age
18 Years
Healthy volunteers
Accepted

Summary

Our randomized controlled double blind clinical trail aims to compare maternal and neonatal infectious morbidity between women with meconium-stained amniotic fluid treated with zinacef vs. placebo.

Detailed description

The relationship between meconium staining and chorioamnionitis, as well as neonatal sepsis, has been documented, yet the precise mechanisms remain unclear. Additionally, the correlation between prolonged labor and meconium staining was described in the past. In light of these findings, our randomized controlled double blind trail aims to compare maternal and neonatal infectious morbidity between women with meconium-stained amniotic fluid treated with zinacef vs. placebo. Additionally, we aimed to assess the distribution of pathogens in chorioamnionitic swab cultures relative to the antibiotic treatment

Conditions

Interventions

TypeNameDescription
DRUGzinacef tretmentprophylactic antibiotic treatment with zinacef
OTHERPlaceboI.V SALINE 100 CC X3/d

Timeline

Start date
2025-02-18
Primary completion
2028-02-13
Completion
2029-02-13
First posted
2025-02-27
Last updated
2025-07-20

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT06849037. Inclusion in this directory is not an endorsement.