Open-Label Safety and Tolerability Study of Oxymorphone for Acute Postoperative Pain in Pediatric Subjects.

PHASE3CompletedINTERVENTIONAL
Enrollment

58

Participants

Timeline

Start Date

February 17, 2009

Primary Completion Date

April 18, 2011

Study Completion Date

April 18, 2011

Conditions
Postoperative Pain
Interventions
DRUG

Oxymorphone IR

Open-label, 2 part, ascending dose, single and multiple dose q4-6 hrs up to 48 hrs

Trial Locations (11)

15213

The Children's Hospital of Pittsburgh, Pittsburgh

17033

Hershey Medical Center, Hershey

20010

Children's Research Institute, Washington D.C.

33607

St. Joseph's Children's Hospital of Tampa, Tampa

37232

Monroe Carell Jr. Children's Hospital at Vanderbilt, Nashville

46202

Indiana University School of Medicine, Indianapolis

72202

Arkansas Children's Hospital, Little Rock

75235

University of Texas Southwestern Medical Center at Dallas, Dallas

80045

The Children's Hospital, Aurora

94305

Stanford University School of Medicine, Stanford

98104

University of Washington, Seattle

Sponsors
All Listed Sponsors
lead

Endo Pharmaceuticals

INDUSTRY