Gabapentin as an Adjunct to Perioperative Pain Management Regimens for Uterine Aspiration
NCT02725710
Abortion, Spontaneous, Female Urogenital Diseases and Pregnancy Complications
Durham, North Carolina, United States
View Trial DetailsNCT Number: NCT02415894
The goal of this study is to examine the effectiveness and feasibility of a mifepristone-misoprostol medical abortion regimen in terminating pregnancies 13-22 weeks in Ukraine.
Looking for future studies?
Notify MeFemale
Observational
Odessa Regional Hospital, Odesa, Ukraine
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 15 hours after start of misoprostol induction
Gynuity Health Projects
Other
Mifepristone and Misoprostol for Mid-trimester Termination of Pregnancy (13-22 Weeks LMP) in Ukraine
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT02725710
Abortion, Spontaneous, Female Urogenital Diseases and Pregnancy Complications
Durham, North Carolina, United States
View Trial Details