Mesh-free prolapse surgery study using vNOTES approach
Part of Women’s health & pregnancy clinical trials.
This trial tests a new surgical method called vNOTES for repairing pelvic organ prolapse without using mesh. It aims to see if this approach improves symptoms and anatomy recovery for women with moderate to severe prolapse.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You are a woman over 18 years old
- You have pelvic organ prolapse at stage 2 or higher (moderate to severe)
- You have symptoms from the prolapse that require surgery
- You have not had any previous cancer treatment like chemotherapy or radiation
- You have not had any prior surgery for prolapse
- You do not have serious heart or lung disease
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 trial compares two minimally-invasive surgical techniques to fix pelvic organ prolapse. It aims to see which method works better and has fewer side effects.
This trial studies how well and how safely a synthetic mesh surgery works for people with pelvic organ prolapse, especially when it causes bladder or urinary problems. It may help find better symptom relief, but it also tracks side effects closely.
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 is a patient registry study for people having a laparoscopic or robotic operation called ventral mesh rectopexy to treat posterior pelvic organ prolapse. It mainly collects information through questionnaires to better understand outcomes and care, rather than testing a new drug.
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.
Hear when a new Pelvic Organ Prolapse trial opens
We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.