Registry for surgery to fix pelvic organ prolapse
Part of Digestive system clinical trials.
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.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You are 18 years or older
- You are scheduled to have laparoscopic or robotic ventral mesh rectopexy for posterior pelvic organ prolapse
- You can give written consent (sign a consent form)
- You are not pregnant at the time of enrollment
- You have an email address so the team can send you questionnaires
- You can complete questionnaires in the required language (or the doctor decides you can)
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 tests how well ventral mesh rectopexy works for people with a full-thickness rectal prolapse. It follows your recovery through questionnaires and check-ups to see if the surgery improves your bowel function and quality of life.
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 registry follows women having pelvic repair surgery that uses synthetic mesh or a synthetic sling. It helps track outcomes over time and may reassure patients that long-term safety and results are being monitored.
This study follows people who have pelvic reconstructive surgery using a trans-vaginal mesh to learn about possible complications over time. It may help improve care by tracking outcomes for up to 36 months.
This study is checking women’s outcomes after a specific prolapse surgery where a mesh material (GYNEMESH PS) was used. If you had this operation and can do follow-up visits, this study may help doctors better understand the mesh’s real-world safety and results.
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