Skip to content

Human Chorionic Gonadotropin (hCG) Trend After Medication Abortion

Human Chorionic Gonadotropin (hCG) Trend After Medication Abortion: A Prospective Physiologic Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02179944
Enrollment
66
Registered
2014-07-02
Start date
2014-07-31
Completion date
2015-03-31
Last updated
2015-08-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Undesired Pregnancy

Keywords

medication abortion, serum hCG

Brief summary

This project will be a prospective physiologic study. We will closely follow 60 medication abortion patients with serial repeat serum hCG and urine semi-quantitative hCG testing. We plan to recruit patients from two gestational age strata: ≤ 49 days and \> 49 days. Study Objectives: 1. To create a nomogram describing the change in serum hCG values in the first five days immediately following medication abortion with mifepristone and misoprostol. Specifically, we will describe the percent serum hCG decline from Day 1 (day of mifepristone) to Day 3 (day after misoprostol), from Day 1 to Day 5, and from Day 1 to Day 7-10. 2. To explore whether there is a significant difference in the rate of hCG decline based on initial gestational age determined by ultrasound and initial serum hCG. 3. To describe the correlation between semi-quantitative urine hCG test results and serum hCG values to determine how soon after initiating medication abortion the urine test can detect completed abortion. We hypothesize that among successful medication abortions, there will be a predictable trend with at least a 50% drop by Day 3 and 80% drop by Day 5.

Interventions

None listed

Sponsors

Planned Parenthood League of Massachusetts
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Desire for medication abortion for pregnancy termination AND * Pregnancy confirmed by ultrasound and gestational age ≤ 63 days based on transvaginal ultrasound (TVUS) OR * Positive high-sensitivity urine hCG and intrauterine pregnancy (IUP) not confirmed on TVUS

Exclusion criteria

* Ineligibility for medication abortion at Planned Parenthood League of Massachusetts (PPLM) based on current PPLM clinical guidelines * Initiation of medication abortion on Wednesday or Friday * Failed pregnancy defined as: * Crown-rump length ≥ 7mm and no heartbeat * Mean sac diameter ≥ 25mm and no embryo * Reasonable clinical suspicion for ectopic or molar pregnancy such as abnormal or concerning ultrasound findings * Multiple gestation * Age less than 18 years * Prior participation in this study * Anticipated inability to present for scheduled follow-up visits

Design outcomes

Primary

MeasureTime frameDescription
Percent serum hCG decline from Day 1 to Day 3, from Day 1 to Day 5, and from Day 1 to Day 7-1010 days from misoprostol administrationblood sample collection for hCG testing on Day 3, Day 5 and Day 7-10 (Day 1 is day of mifepristone administration)

Secondary

MeasureTime frameDescription
difference in rate of hCG decline based on initial gestational age10 days after misoprostol administrationblood sample collection for hCG testing on Day 3, Day 5 and Day 7-10 (Day 1 is day of mifepristone administration)

Other

MeasureTime frameDescription
how soon after initiating medication abortion a semi-quantitative urine pregnancy test can detect completed abortion10 daysurine sample collection for hCG testing using semi-quantitative urine pregnancy test on Day 1, Day 3, Day 5 and Day 7-10 (Day 1 is day of mifepristone administration)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026