Clin2
NCT05042453Possibly a fitRecruiting

Long-term follow-up of Splentis for uterine prolapse repair

Pelvic Organ Prolapse

Part of Kidney & urinary, Women’s health & pregnancy clinical trials.

This trial follows women who have symptoms of uterine prolapse and are getting surgery with a device called Splentis. The study looks at whether Splentis works over the long term and whether it has any important side effects.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
140 people
Ages
18 years and older
Study type
Observational

Who can take part

  • You are a woman who is not planning to have children (non-fertile).
  • You have a first-time (primary) case of uterine prolapse with symptoms (descent at a certain measurement level).
  • You are scheduled for apical prolapse repair surgery and the surgeon plans to use Splentis.
  • You are willing and able to attend study visits and sign informed consent.
  • You should not have a known allergy to polypropylene (a material related to the device).

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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