Clinical Trials Directory

Trials / Completed

CompletedNCT02277249

Transvaginal Versus Transabdominal Digoxin Prior to Second-trimester Abortion

Transvaginal Versus Transabdominal Digoxin Prior to Second-trimester Abortion: a Pilot Study of Patient Preference

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
University of California, Los Angeles · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Accepted

Summary

Current practice for the provision of late second trimester abortion (dilation and evacuation, or D\&E) often involves the administration of digoxin into the fetal compartment to induce fetal demise prior to the procedure. Digoxin may be administered transabdominally or transvaginally into the fetal compartment. Both modes of administration have been shown in prospective studies to be highly effective and safe. Both modes of administration are considered standard of care. This pilot study will directly compare transabdominal and transvaginal digoxin with respect to patient preference (i.e, patient pain score describing discomfort with injection).

Conditions

Interventions

TypeNameDescription
DRUGDigoxin (transvaginal administration)Transvaginal digoxin administration prior to second-trimester abortion. This is only listed as a "Procedure/Surgery" type intervention because the mode of digoxin administration (transvaginal versus transabdominal) is what is being studied.
DRUGDigoxin (transabdominal administration)Transabdominal digoxin administration prior to second-trimester abortion. This is only listed as a "Procedure/Surgery" type intervention because the mode of digoxin administration (transvaginal versus transabdominal) is what is being studied.

Timeline

Start date
2012-10-01
Primary completion
2014-10-01
Completion
2014-10-01
First posted
2014-10-28
Last updated
2017-01-13
Results posted
2016-10-19

Source: ClinicalTrials.gov record NCT02277249. Inclusion in this directory is not an endorsement.