Evaluate whether the 4K laparoscopic vision system can provide an advantage in performing bilateral oophorectomy procedures for benign conditions carried out by trainee surgeons compared to 3D laparoscopy

All patients diagnosed with suspected benign ovarian pathology based on preoperative examinations (pelvic Doppler ultrasound and/or magnetic resonance imaging and/or CT scan) and with indication for bilateral laparoscopic adnexectomy will be enrolled in the study. The primary objective of the study is to compare surgical times between the 3D and 4K vision systems in laparoscopic ovarian surgery, specifically in bilateral adnexectomy performed by trainee surgeons. Secondary objectives will include evaluating intra- and postoperative complications, length of hospital stay, and costs to the healthcare system

Inclusion Criteria:

• Patients with benign ovarian pathology requiring bilateral oophorectomy
• ASA score <3
• Patients who have signed the appropriate informed consent
• Patients who are not pregnant or diagnosed with pelvic inflammatory disease
• No history of prior major abdominal surgery

Exclusion Criteria:

• Suspected neoplastic pathology
• Patients not eligible for surgery