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Clinical Trial Summary

This study aims to compare the routine use versus non-use of urethral catheterization in women undergoing first elective cesarean section as regard to intraoperative and postoperative complications


Clinical Trial Description

This randomized controlled trial will be done at Ain Shams University Maternity One hundred and seventy pregnant women scheduled for first elective CS attending at outpatient clinic will be chosen after complete history and physical examination to determine eligibility for inclusion after taking their consent with full explanation of the study including potential benefits and risks.

The study population will be randomized using computer sequence program in 1:1 ratio. Allocation of every patient to one of the studied groups will be done using opaque envelops.

The studied groups will be either Group C or Group N For both groups

- A written consent will be taken.

- Full history to exclude medical problems that need special care.

- Full history to exclude UTI or recurrent UTI during pregnancy.

- A single dose of 2 gm cefazolin will be given IV pre-incision for preoperative antibiotic prophylaxis (Sullivan et al., 2007).

- midstream urine samples will be collected preoperative to exclude UTI and 24 hours postoperatively after giving the instructions to the patients (washing hands and genitals ,pass some urine into the toilet then without stopping catch some urine in a sterile container ) to be analyzed for presence of UTI ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03459963
Study type Interventional
Source Ain Shams Maternity Hospital
Contact
Status Active, not recruiting
Phase N/A
Start date May 18, 2017
Completion date April 1, 2018

See also
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