Expediting Pregnancy of Unknown Location Risk Stratification Using the ROM-Plus Point of Care Test

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age15+
SponsorUniversity of California, Davis

About this trial

The goal of this study is to learn if the ROM-Plus bedside test can effectively triage patients who present with pregnancy of unknown location (PUL) and vaginal bleeding as high or low risk for ectopic pregnancy. The main question to answer is:

Can the ROM-Plus bedside test effectively risk-stratify patients who present with PUL and vaginal bleeding as high or low risk for ectopic pregnancy after a single clinical encounter.

Participants will have a vaginal swab collected at the time of presentation.

Eligibility criteria

Qualifiers

PUL diagnosis in the UC Davis Emergency Department or Obstetrics and Gynecology Office

Vaginal bleeding

Clinically stable

English-speaking

Disqualifiers

None

Trial design

Treatments tested in this trial

  • ROM-Plus bedside test

Treatment groups

122 Participants
are divided into 1 treatment group

Locations

This trial has no locations

Sponsors and collaborators

University of California, Davis

Lead sponsor

Laborie Medical Technologies Inc.

Collaborator