Sponsor:
Fertility Specialists of Houston
Code:
NCT01549171
Conditions
Pregnancy
Eligibility Criteria
Sex: Female
Age: 20 - 39
Healthy Volunteers: Not accepted
Interventions
Iloprost
normal saline
Brief summary:
Conditions
Pregnancy
Study ID
NCT01549171
Start date
Jan, 2010
Status verified date
Mar, 2012
Completion date
Dec, 2013
Anticipated
Primary completion date
Nov, 2011
Eligibility Criteria
Sex: Female
Age: 20 - 39
Healthy Volunteers: Not accepted
Enrollment
100 participants
Anticipated
Arms
Iloprost
Control
Interventions
Iloprost
normal saline
Primary outcome measure
Locations
Fertility Specialists of Houston
Recruiting
Houston, Texas, United States, 77054
Contacts
Sponsor
Fertility Specialists of Houston
Last update posted
Mar 9, 2012
Last verified
Mar, 2012
Keywords
Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Fertility Specialists of Houston on 2012-03-09.