Ulcerative Colitis Clinical Trials

Showing 6501-6520 of 7,290 trials

Recombinant Human Relaxin (rhRlx) in Pregnant Women Scheduled for Induction of Labor

NCT00259103

The purpose of this study is to assess the safety and efficacy of rhRlx for cervical ripening, when compared to a placebo.

Labor, Induced

Corthera, Inc.(formerly BAS Medical, Inc.), a member of the Novartis group of companies72 participantsStarted Nov 2005

Novosibirsk, Russia • Saint Petersburg, Russia • Saint Petersburg, Russia

COMPLETEDPhase 1

A Single Centre Study to Evaluate 3 Ophthalmic Formulations in Healthy Subjects

NCT02003547

A Single Centre, Placebo-Controlled, Double-Masked, Sequential Designed Study to Evaluate 3 Ophthalmic Formulations of AMA0076 in Healthy Subjects

GlaucomaOcular HypertensionEye Disease

Amakem, NV21 participantsStarted Sep 2013

Ruddington, Nottingham, United Kingdom

COMPLETEDPhase 3

Efficacy & Safety Study Comparing Misoprostol Vaginal Insert (MVI) Versus Dinoprostone Vaginal Insert (DVI) for Reducing Time to Vaginal Delivery

NCT01127581

The purpose of this study is to determine whether the Misoprostol Vaginal Insert (MVI) 200 microgram (mcg) can decrease the time to vaginal delivery compared to the Dinoprostone Vaginal Insert (DVI) 10 milligram (mg) in pregnant women requiring cervical ripening and induction of labor.

Reducing Time to Vaginal DeliveryCervical RipeningInduction of Labor

Ferring Pharmaceuticals1,358 participantsStarted Sep 2010

Phoenix, Arizona, United States • Phoenix, Arizona, United States • Scottsdale, Arizona, United States +31 more locations

Recombinant Human Relaxin (rhRlx) in Pregnant Women Scheduled for Induction of Labor

A Single Centre Study to Evaluate 3 Ophthalmic Formulations in Healthy Subjects

Efficacy & Safety Study Comparing Misoprostol Vaginal Insert (MVI) Versus Dinoprostone Vaginal Insert (DVI) for Reducing Time to Vaginal Delivery

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