Safety Study of Pelvic Organ Prolapse Repair Using Transvaginal Mesh

PHASE2/PHASE3CompletedINTERVENTIONAL
Enrollment

250

Participants

Timeline

Start Date

August 31, 2006

Study Completion Date

March 31, 2007

Conditions
Pelvic Organ Prolapse
Interventions
DEVICE

Transvaginal mesh- PROLIFT®-system

Trial Locations (26)

Unknown

Nyköbing Hospital, Nyköbing

Skejby Hospital, Skejby

Jorvi Hospital, Jorvi

Lahti Hospital, Lahti

Lojo Hospital, Lohja

Åbo Hospital, Turku

Akershus University Hospital, Ahus

Haukeland Hospital, Bergen

Bærum Hospital, Bærum

Gjøvik Hospital, Gjøvik

Kongsberg Hospital, Kongsberg

Rikshospitalet, Oslo

The Regional Hospital in Tromsø, Tromsø

Sahlgrenska Hospital, Gothenburg

Halmstad Hospital, Halmstad

Kristiansstad Hospital, Kristiansstad

Linköping University Hospital, Linköping

Vrinnevi Hospital, Norrköping

Örebro University Hospital, Örebro

Skaraborg Hospital Skövde, Skövde

Danderyd University Hospital, Stockholm

S:t Göran Hospital, Stockholm

South Hospital, Stockholm

Uppsala Academic Hospital, Uppsala

Västerås Hospital, Västerås

Ystad Hospital, Ystad

All Listed Sponsors
collaborator

Karolinska University Hospital

OTHER

lead

Karolinska Institutet

OTHER

NCT00402844 - Safety Study of Pelvic Organ Prolapse Repair Using Transvaginal Mesh | Biotech Hunter | Biotech Hunter