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Clinical Trial Summary

The investigators assess in this study the sensitivity of Urea and Creatinine and that of Nitrazine test in vaginal wash after injecting saline in the vagina of patients with pre-labour rupture of membranes


Clinical Trial Description

The aim of this study is to compare the accuracy of measuring the urea and creatinine level versus that of nitrazine test in vaginal wash of pre-labour rupture of membranes patients.Each patient with rupture of membranes will be assessed clinically and then if not in labour , patients will be divided into 2 groups, 5ml saline will be injected in the vagina of each patient in every group then the vaginal wash will be collected in a test tube. Urea and creatinine group, biochemical tests for urea and creatinine in mIU/ml to detect their presence in the wash will be done. In Nitrazine group wash will be assessed by nitrazine paper showing bluish discoloration in rupture membranes. Sensitivity of each test in diagnosed rupture of membranes will be assessed.Which means how many patients in each test show positive results in case of diagnosed case. ;


Study Design


Related Conditions & MeSH terms

  • Disorder of Amniotic Cavity and/or Membrane
  • Fetal Membranes, Premature Rupture
  • Rupture

NCT number NCT02111148
Study type Interventional
Source Beni-Suef University
Contact Nesreen A Shehata, MD
Phone 00201024150605
Email nesoomar@yahoo.com
Status Recruiting
Phase N/A
Start date May 2014
Completion date December 2021

See also
  Status Clinical Trial Phase
Completed NCT01309308 - Sweeping the Membranes, Cervical Length and Duration of Labor N/A