National Registry for Surgical and Cryoablation Treatment of Parietal Endometriosis in Women

What this Trial Is About

This research aims to create a national registry for patients suffering from parietal endometriosis, a condition involving nodules in the abdominal wall. It is conducted by a multidisciplinary radiosurgery team and focuses on patients treated with either surgical removal or percutaneous cryoablation. The study will follow participants for three years after treatment to gather comprehensive data on this condition. Patients with parietal endometriosis will be recorded in the registry based on their treatment type either cryoablation or surgery. The study does not involve experimental treatment but observes patients undergoing these procedures. The registry will collect information throughout the treatment and follow-up period, capturing data at multiple time points including one month, six months, one year, two years, and three years after treatment. Participants will be monitored regularly with clinical evaluations, imaging tests such as MRI and ultrasound, and quality of life questionnaires to assess treatment effects and complications. The study will track the epidemiology, imaging characteristics, aesthetic impact, complication rates, and recurrence of nodules. Safety assessments and quality of life measures will be collected throughout the three-year follow-up to understand long-term outcomes of the treatments.

National Registry of Surgical Treatment and Percutaneous Cryoablation of Parietal Endometriosis