Medical Abortion Clinical Trial
— MASCOfficial title:
Medication Abortion Self-Confirmation (MASC): Comparison of Two Home Pregnancy Tests as an Alternative to Office Follow-up
NCT number | NCT03148587 |
Other study ID # | 39816 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | May 1, 2017 |
Est. completion date | May 31, 2018 |
Verified date | June 2019 |
Source | Stanford University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study aims to investigate the ability of participants to perform and accurately interpret the multi-level pregnancy test and the low sensitivity pregnancy test following medication abortion, without routine provider contact.
Status | Completed |
Enrollment | 88 |
Est. completion date | May 31, 2018 |
Est. primary completion date | May 31, 2018 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Gestational age of less than or equal to 63 days - English speaking - Determined by the site investigator or designee to be fully eligible for medical abortion with mifepristone followed by misoprostol according to the site's standard criteria - In the judgement of the site investigator, she is capable of giving informed consent and she has signed the study informed consent or assent form Exclusion Criteria: - Allergy to mifepristone and/or misoprostol - Non-english speaking - Inability to access internet |
Country | Name | City | State |
---|---|---|---|
United States | Stanford Health Care | Stanford | California |
Lead Sponsor | Collaborator |
---|---|
Stanford University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Correct interpretation of pregnancy test | 4 weeks after taking medication abortion medication, mifepristone |
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