Imaging of the Urinary Tract |
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Clinical Trial: Peripartum Bacteruria and UTI
This study is currently recruiting patients.
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Purpose
In the last years Urinary tract infections (UTI) and pyelonephritis have been the most common reason for readmission to our hospital after birth. UTI is know to be one of the leading causes of post partum fever affecting about 3%-8% of all postpartum women.
We hypothesized that collecting urine cultures pre and postnatally may help identify women at risk for developing UTI, while treating women with positive cultures, could decrease the rehospitalization rate due to post-partum fever. Collecting data during delivery may help identify women at risk for this complication.
| Condition | Intervention |
|---|---|
| Urinary Tract Infection Postpartum Period | Procedure: urine culture Drug: antibiotics according to culture |
MedlinePlus related topics: Urinary Tract Infections
Study Type: Interventional
Study Design: Prevention, Randomized, Open Label, Historical Control, Parallel Assignment
Official Title: Risk Factors for Postpartm Bacteruria, Does Labor Cause UTI?
Expected Total Enrollment: 1000
Study start: January 2004; Expected completion: December 2005
Last follow-up: June 2005; Data entry closure: August 2005
The study is planned as a randomized controlled study with 500 women in each arm. The study group will have pre and post labor urine cultures taken, and the risk factors during delivery will be documented, while the control group will have no cultures taken, as the common practice prior to the study.
Women with positive cultures will be contacted by telephone, and antibiotic treatment recommended according to bacteria sensitivity. All women will be contacted by telephone 1 month post partum and data regarding urinary tract symptoms and need for hospitalization, will be collected. The rehospitalization rate will be documented and compared between the two groups.
Our assumption is that routine urine culture to women in the peripartum period may reduce the UTI rate and hospitalization after delivery.
Eligibility
Accepts Healthy Volunteers
Inclusion Criteria: parturients planned for vaginal delivery
Exclusion Criteria: patrturients receiving antibiotic treatment during delivery or in the week before
Location and Contact Information
Hadas Lemberg, PhD 00 972 2 6777572 lhadas@hadassah.org.il
Israel
Obs&Gyn Hadassah Ein-Kerem Medical center, Jerusalem, Israel; Recruiting
David Mankuta, MD, Sub-Investigator
Clinical microbiology, Hadassah Ein-Kerem Medical centre, Jerusalem, Israel; Recruiting
Mervin Shapiro, MD, Principal Investigator
Tamar Elram, MD, Principal Investigator, Hadassah Medical Organization
More Information
Record last reviewed: September 2003
Last Updated: July 25, 2005
Record first received: July 21, 2005
ClinicalTrials.gov Identifier: NCT00121797
Health Authority: Israel: Israeli Health Ministry Pharmaceutical Administration
ClinicalTrials.gov processed this record on 2005-07-26

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