Anchorsure device check for prolapse surgery safety and performance
Part of Women’s health & pregnancy clinical trials.
This trial evaluates how well and how safely the Anchorsure transvaginal device works when used to suspend (support) the top part of the vaginal area during surgery for apical pelvic organ prolapse. It may help improve surgical outcomes and identify risks for people like you needing this type of prolapse operation.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You have pelvic organ prolapse where the main bulge reaches at least the hymen area (measured on a standard prolapse scale).
- Your planned surgery is for apical prolapse using the Anchorsure System—either alone or with other planned procedures (like native tissue repair, hysterectomy, or a sling for leakage).
- You agree to take part and you understand the study information.
- You have not joined another drug or device study in the last 3 months (other than a specific mesh registry).
- You do not have uncontrolled diabetes, ongoing uncontrolled infections, or tissue damage that makes surgery unsafe.
- You do not have pelvic cancer now, past pelvic radiation, immune-suppressing medicines in the last month, or you are not on blood thinners (oral anticoagulants).
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
Similar studies
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This trial tests a new material made from donated human tissue to repair pelvic organ prolapse. It may help women with certain types of prolapse who have not had prior pelvic surgery.
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This study tests a new mesh implant to fix pelvic organ prolapse (when organs drop down into the vagina). It looks at how safe and well the implant works in women who need surgery for this condition.
This trial compares two surgical options to treat a type of vaginal prolapse where the top of the vagina (apical area) has dropped. It may help find which approach works better and has fewer long-term problems for people who’ve had prior prolapse surgery and a hysterectomy.
This study checks whether an outpatient (same-day) approach to a specific prolapse repair surgery is safe and practical, using a double-mesh method with or without robotic help. You may be offered the surgery under guidance of the study team if you meet the health and medical safety criteria.
This trial tests whether using vaginal estrogen before and after prolapse surgery helps improve recovery and long-term results. Women having apical suspension surgery (to support the top of the vagina) may benefit.
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