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 compares a biological mesh made from sheep tissue (OviTex) with a standard synthetic mesh for repairing pelvic organ prolapse during robotic surgery. It aims to see which one works better and has fewer side effects.
This study looks at how well patients recover after a specific surgery for rectal prolapse, called ventral mesh rectopexy. It aims to understand the functional outcomes to help improve care for future patients.
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 trial is a follow-up for women who were already part of an earlier randomized study. It looks at how well the vaginal mesh surgery works over the long term and whether it continues to help symptoms safely.
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