i-Stitch for pelvic organ prolapse support surgery
Part of Women’s health & pregnancy clinical trials.
This study tests a device called i-Stitch for women having surgery to fix pelvic organ prolapse. It may help repair the pelvic area by securing the vagina in place with a special tool.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You are having surgery for pelvic organ prolapse.
- Your doctor plans to use the i-Stitch device to do the repair.
- You are at least 18 years old.
- You agree to sign a consent form for the surgery.
- You do not have an active or hidden infection.
- You do not have allergic reactions to the materials in the device.
- You do not have bleeding or clotting problems.
- You do not have autoimmune connective tissue disease.
- You do not have any problems with your uterus.
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
Other trials that look related to this one.
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 study compares two surgical techniques to repair pelvic organ prolapse (when organs like the bladder or bowel sag into the vaginal area). It aims to see which method gives better support with fewer risks, potentially offering you a lasting fix.
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 compares two surgical techniques to repair pelvic organ prolapse (when organs like the bladder or uterus push into the vagina). One method uses a synthetic mesh, and the other uses a natural stitch to hold the organs in place. Both surgeries involve removing the uterus (if you still have one), and the goal is to see which approach works better and has fewer complications.
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.
This trial compares two surgical ways to support the uterus without removing it: a vaginal approach versus a laparoscopic (camera) approach. It may help you choose the method that best improves uterine prolapse symptoms and function.
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