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Vaginal Fluid Wash in Pre-labour Rupture of Membranes

NCT02111148 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 105

Last updated 2021-02-16

No results posted yet for this study

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

Conditions

  • Disorder of Amniotic Cavity and/or Membrane

Interventions

PROCEDURE

Urea and creatinine

the vagina will be washed with 5ml saline, urea and creatinine will be detected biochemically in the vaginal wash.

PROCEDURE

Nitrazine

Nitrazine detection in vaginal wash

DRUG

5ml saline

the vagina will be washed with 5ml saline and vaginal wash will be collected.

Sponsors & Collaborators

  • Cairo University

    collaborator OTHER

  • Beni-Suef University

    lead OTHER

Principal Investigators

  • Nesreen A Shehata, MD · Beni-Suef University

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
30 Years
Max Age
40 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-05-31
Primary Completion
2021-12-31
Completion
2021-12-31

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02111148 on ClinicalTrials.gov