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Clinical trial

Development of a Rapid Amniotic Fluid (AF) Test and a Non-Invasive Vaginal Fluid (VF) Test to Detect Intra-Amniotic Infection and Predict Preterm Birth in Women Presenting With Preterm Labor and Intact Amniotic Membranes

NCT03497234 is registered in ClinicalTrials.gov with Hologic, Inc. as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
Development of a Rapid Amniotic Fluid (AF) Test and a Non-Invasive Vaginal Fluid (VF) Test to Detect Intra-Amniotic Infection and Predict Preterm Birth in Women Presenting With Preterm Labor and Intact Amniotic Membranes
Lead sponsor
Hologic, Inc.
Phase
Not applicable
Overall status
Withdrawn
Start date
March 28, 2018
Completion date
March 31, 2020
Enrollment
0 (actual)
Sites
5

Conditions

As the registry lists them; a condition with its own page is linked.

intra-amniotic infection of foetus