Group B Streptococcus Infection and PROM Incidince

ConditionsPremature Rupture of Fetal Membranes Group B Streptococcal Infection

Trial statusNot yet recruiting

Trial phaseNot listed

Trial typeObservational

Biological sexFemale

AgeNot listed

SponsorAssiut University

About this trial

To investigate incidince of prom with GBS infection and role of prophylaxis against it

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Pregnant women with prom after 34 wks festation

Disqualifiers

Bleeding disorder

emergency conditions

Trial population

Pregnant women with prom

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

To provide ampicillin sulbactam to pregnant women with premature rupture of membrane
Drug
To provide ampicillin sulbactam tonpregnant women with premature rupture of membrane after 34 wks gestation

Treatment groups

150 Participants

are divided into 1 treatment group

Group A: Pregnant women after 34 wks with PROM1 intervention

Trial outcomes

Primary outcomes

Incidince of prom with GBS infection and prophylaxis against it

Time frame

Baseline

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Assiut University

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: