Comparing Intra-Abdominal Pressure During Gynecologic Laparoscopy

The goal of this clinical trial is to learn if the level of intra-abdominal pressure during benign gynecologic laparoscopic surgery impacts postoperative pain. The main question it aims to answer is: • Does use of low (8 mmHg) versus standard (15 mmHg) intra-abdominal pressure impact postoperative pain? Researchers will compare the use of low (8 mmHg) versus standard (15 mmHg) intra-abdominal pressure. Participants will: * Undergo their regular scheduled gynecologic laparoscopic surgery * Complete pain measures one hour, 3 hours, and 24 hours after surgery

Inclusion Criteria: * Undergoing benign gynecologic laparoscopic surgery with eligible procedures, including the following. * Salpingectomy * Cystectomy * Oophorectomy * Myomectomy * Hysterectomy. * Only those who speak English or Spanish will be recruited, as our validated questionnaires are only available in those languages. Exclusion Criteria: * Participants with the following diseases will be excluded due to their diseases having pain that may strongly interfere with their perception of pain in the area of surgery. * Arthritis * Gout * Metastatic cancer * Pelvic floor disease * Headache disorders * Herpes zoster or shingles * Frozen shoulder * Complex regional pain syndrome (CRPS) * Slipped disc * Sickle cell disease * Sciatica * Trigeminal neuralgia * Fibromyalgia.