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Clinical Trials/NCT05469984
NCT05469984
Recruiting
Not Applicable

Comparing Obstetrical Outcomes and Infectious Morbidity Between Two Prophylactic Antibiotic Protocols in Women With Term Prolonged Pre-labor Rupture of Membrane and Preterm Labor

Western Galilee Hospital-Nahariya1 site in 1 country600 target enrollmentNovember 25, 2022

Overview

Phase
Not Applicable
Intervention
Ampicillin Only Product
Conditions
Preterm Labor With Preterm Delivery
Sponsor
Western Galilee Hospital-Nahariya
Enrollment
600
Locations
1
Primary Endpoint
endometritis rate
Status
Recruiting
Last Updated
8 months ago

Overview

Brief Summary

This randomized prospective trial aimed to compare 2 prophylactic antibiotic regiment (ampicillin alone versus ampicillin plus gentamycin) in term prolonged pre-labor rupture of membrane and in preterm deliveries and examine related obstetrical outcome and infectious morbidity

Detailed Description

Maternal peripartum fever is a common complication of pregnancy and postpartum period associated with potentially serious obstetrical outcomes and infectious morbidity. Peripartum infections includes intrapartum intraamniotic infection (IAI) and postpartum endometritis. Both are caused by polymicrobial bacterial infection. Increased latency period from rupture of membranes (ROM) until delivery is a common risk factor. Another risk factor is pre-term delivery. This randomized prospective trial aimed to compare 2 prophylactic antibiotic regiment (ampicillin alone versus ampicillin plus gentamycin) in term prolonged pre-labor rupture of membrane and in preterm deliveries and examine related obstetrical outcome and infectious morbidity. Primary outcome-peripartum infections- chorioamnionitis, endometritis and surgical site infection secondary outcome- obstetrical outcome- mode of delivery, Apgar score, cord blood pH, peripartum fever, maternal length of admission, postpartum maternal antibiotic treatment, Surface swab cultures were obtained from the placenta, amnion and umbilical cord (birth cultures) and uterine swab cultures, maternal blood culture, placental histologic evaluation neonatal outcomes-NICU admission, length of admission, neonatal morbidity-ventilation support, early neonatal sepsis

Registry
clinicaltrials.gov
Start Date
November 25, 2022
End Date
September 26, 2025
Last Updated
8 months ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dr. Maya Wolf

Director- Fetal Maternal Medicine Unit

Western Galilee Hospital-Nahariya

Eligibility Criteria

Inclusion Criteria

  • maternal age \> 18 years singleton pregnancy vertex presentation prolonged \>18 h prom or preterm delivery

Exclusion Criteria

  • GBS carrier
  • preterm premature rupture of membrane for conservative treatment
  • intra-uterine fetal death fetal major anomaly
  • drug allergy for the antibiotic in use in this study
  • women receiving antibiotic treatment for other infection such as urinary tract infection

Arms & Interventions

women with term prolonged>18h rupture of membrane

women with term prolonged \>18 h prom or in preterm delivery will be treated with IV ampicillin 2 gr every 6 hours until delivery

Intervention: Ampicillin Only Product

women with term prolonged>18h rupture of membrane

women with term prolonged \>18 h prom or in preterm delivery will be treated with IV ampicillin 2 gr every 6 hours until delivery

Intervention: ampicillin plus gentamicin

women with preterm labor

women with term prolonged \>18 h prom or in preterm delivery will be treated with IV ampicillin 2 gr every 6 hours until delivery plus IV gentamicin 5 mg/kg every 24 hours

Intervention: Ampicillin Only Product

women with preterm labor

women with term prolonged \>18 h prom or in preterm delivery will be treated with IV ampicillin 2 gr every 6 hours until delivery plus IV gentamicin 5 mg/kg every 24 hours

Intervention: ampicillin plus gentamicin

Outcomes

Primary Outcomes

endometritis rate

Time Frame: up to 6 weeks postpartum

chorioamnionitis rate

Time Frame: during labor (up to delivery of the newborn)

Secondary Outcomes

  • cord blood pH(immediately after delivery of the placenta)
  • maternal intrapartum fever(during labor (up to delivery of the newborn))
  • NICU (neonatal intensive care unit) hospitalization length,(up to 3 month from delivery)
  • rate of neonatal early onset sepsis(up to one week from delivery)
  • Rate of participants treated with antibiotics during the postpartum period(6 week postpartum)
  • maternal postpartum hospitalization length(up to 6 weeks post partum)
  • Number of neonate with ventilation support(one week from delivery)
  • Number of neonate treated with antibiotics(one week from delivery)

Study Sites (1)

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