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Amniotic Fluid Lactate in Perterm Premature Rupture of Membranes

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ClinicalTrials.gov Identifier: NCT03789903
Recruitment Status : Recruiting
First Posted : December 31, 2018
Last Update Posted : December 31, 2018
Sponsor:
Information provided by (Responsible Party):
Radwa Rasheedy Ali, Ain Shams University

Brief Summary:
AF lactate level could help in predicting the duration from ROM till delivery

Condition or disease Intervention/treatment Phase
Rupture of Membranes; Premature Diagnostic Test: amniotic fluid lactate Not Applicable

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 80 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Diagnostic
Official Title: Amniotic Fluid Lactate in Predicting Latency in Perterm Premature Rupture of Membranes
Actual Study Start Date : January 1, 2018
Estimated Primary Completion Date : January 1, 2019
Estimated Study Completion Date : March 1, 2019

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Tears


Intervention Details:
  • Diagnostic Test: amniotic fluid lactate
    AF lactate


Primary Outcome Measures :
  1. latency period [ Time Frame: upto 48 hours ]
    duration from ROM till the occurrence of active labor



Information from the National Library of Medicine

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Ages Eligible for Study:   25 Years to 35 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. women with PPROM
  2. GA between 24 to 34 weeks

Exclusion Criteria:

  1. chorioamnionitis
  2. previous Preterm labor
  3. abruptio placentae
  4. UTI ,pyelonephritis

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03789903


Contacts
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Contact: Radwa R Ali, MD 01283492979 ext 02002 radwaebed@yahoo.com

Locations
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Egypt
AinShams university maternity hospital Recruiting
Cairo, Abbassya, Egypt, 11566
Contact: Ahmed K Maklad, MD         
Sponsors and Collaborators
Ain Shams University

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Responsible Party: Radwa Rasheedy Ali, Principal Investigator, Ain Shams University
ClinicalTrials.gov Identifier: NCT03789903     History of Changes
Other Study ID Numbers: ain shams maternity hos
First Posted: December 31, 2018    Key Record Dates
Last Update Posted: December 31, 2018
Last Verified: December 2018

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Premature Birth
Fetal Membranes, Premature Rupture
Rupture
Obstetric Labor, Premature
Obstetric Labor Complications
Pregnancy Complications
Wounds and Injuries