Novel Diagnosis of Ectopic Pregnancy

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-45
SponsorAcibadem University

About this trial

In the project, the investigators aim to determine the Beta- human chorionic gonadotropin (BHCG) value with serial measurements on the same day in the diagnosis of ectopic pregnancy.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Positive bhcg levels

Disqualifiers

clinically diagnosis of intrauterine pregnancy

Trial design

Design model

Parallel

Treatments tested in this trial

  • serum BHCG testing

    Diagnostic test

    Taking 5ml blood samples every 2 hours for 5 times for measurement of BHCG. Blood samples will be taken from the median cubital and cephalic veins which is located inner side of the elbow.

Treatment groups

20 Participants
are divided into 2 treatment groups
Group A: ectopic pregnancy patientsExperimental treatment 1 intervention
Group B: Normal pregnancyActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Changes in Beta-hCG Levels Measured Every 2 Hours as a Discriminating Factor Between Ectopic and Normal Pregnancy

The primary outcome is how the changes in Beta-hCG levels measured every two hours differ between the ectopic pregnancy and the normal pregnancy.

Time frame
10 hours

Secondary outcomes

1

Increase pattern of BHCG levels in normal pregnancy

BHCG increase pattern every two hours in normal pregnancy

Time frame
10 hours

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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