Intrafetal Digoxin as an Adjuvant for Dilation and Evacuation at 20 to 24 Weeks' Gestation
Completed · Phase 4 · Has a placebo group
Conditions studied: Abortion
In brief
This is a research study to measure the effect of digoxin injection on Dilation and Evacuation (D\&E) procedure duration. Digoxin is the most commonly used feticidal agent among family planning subspecialists, and is commonly used for a variety of reasons including provider preference, patient preference, and concerns over legal status of later D\&E procedures. There have been several studies on digoxin administration, adverse effects, and impact on the D\&E procedure, but doctors want to clarify how digoxin effects D\&E procedure time, if at all.
Key facts
- Study ID
- NCT03136068
- Run by
- University of California, San Francisco
- People needed
- 178
- Starts
- 2017-02-23
- Expected to finish
- 2018-05-31
- Last updated by the study team
- 2019-10-30
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- 20 weeks 0 days-24 weeks 0 days gestation
- English or Spanish speaking
- 18 years or older
You may not qualify if…
- Under 18
- Contraindications to digoxin
Where it is running
- FPA Women's Health — Long Beach, California, United States
- SFGH Women's Options Center — San Francisco, California, United States
- Lovejoy Surgicenter — Portland, Oregon, United States
Full record on ClinicalTrials.gov
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