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Clinical trial

PDS (Polydiaxonene Suture) Versus Prolene (Polypropylene Suture) as Suture Material for Vaginal Sacrospinous Hysteropexy - a Randomised Controlled Study

NCT05964881 is registered in ClinicalTrials.gov with Medical University of Vienna as lead sponsor.

NCT NCT05964881
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Registry record

As filed in ClinicalTrials.gov.

Title
PDS (Polydiaxonene Suture) Versus Prolene (Polypropylene Suture) as Suture Material for Vaginal Sacrospinous Hysteropexy - a Randomised Controlled Study
Lead sponsor
Medical University of Vienna
Phase
Not applicable
Overall status
Unknown status
Start date
May 15, 2023
Completion date
December 31, 2025
Enrollment
52 (estimated)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

pelvic organ prolapse, prolapse