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Clinical Trials in Sweden / NCT07417787
Recruiting Observational

Point of Care Tests in the Management of Very Early Medical Abortion

NCT07417787 · tracked via the Priya Life Science Sweden tracker
Phase
Observational
Started
2026-04-23
Last updated
2026-06-03

Condition(s) studied

Abortion Early

Investigational drug(s) / intervention(s)

Blood testParticipant Questionnaire

Blood test: Patients will undergo one additional blood test than is usual with standard care, to measure Human Chorionic Gonadotropin (HCG) level which will be analysed on a point of care test machine and in the lab

Participant Questionnaire: The investigators will administer participant questionnaires to both staff and patients to understand opinions on the point of care test machine

Study summary

This study will investigate the use of a point of care test in patients who are having an abortion at a gestation of \<6 weeks (known as a very early medical abortion). These patients have pregnancy hormone level checked at Day 0 and Day 7 to see if treatment has worked. The investigators plan to use a point of care test machine to see if it is possible to check pregnancy hormone level earlier than Day 7.

Eligibility

Sex
FEMALE
Min age
16 Years
Max age
55 Years
Healthy volunteers
No
Inclusion Criteria: * Positive pregnancy test * Less than six weeks gestation based upon Last Menstrual Period (LMP) * No evidence of definite intrauterine pregnancy on ultrasound * No signs or symptoms or significant risk factors for ectopic * Wish to proceed to VEMA (Very Early Medical Abortion) * Available for usual clinical follow up * Willing to attend for serum Human Chorionic Gonadotropin (HCG) on two occasions Day 2-4 and Day 7 post mifepristone * Written informed consent Exclusion Criteria: * Pain and/or bleeding * Significant risk factors for ectopic (previous ectopic, sterilisation, tubal disease, intrauterine device in situ) * Suspicious features for ectopic on ultrasound (adnexal mass, moderate free fluid) * Unable to provide blood sample * Lack of Capacity to consent

Primary outcome measure(s)

Trial sites (3)

FacilityCityRegionStatus
University of Gothenberg Gothenburg Sweden Not Yet Recruiting
Karolinska Institutet Stockholm Sweden Not Yet Recruiting
Chalmers Sexual Health Clinic Edinburgh United Kingdom Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07417787 on ClinicalTrials.gov ↗ ← All trials in Sweden