About this trial
The goal of this clinical trial is to evaluate the incidence and severity of post-operative shoulder pain following elective robot-assisted hiatal hernia repair in hopes of reducing pain and associated costs as well as clinic and emergency department visits due to this pain. You will undergo standard robot-assisted hiatal hernia repair with the standard postoperative care. The only difference is that you may be selected for the group where lower pressures used to fill your abdomen with carbon dioxide will be used, and you will be asked to fill out logs regarding your pain postoperatively. You will have postoperative appointments that are standard following this procedure.
Eligibility criteria
Qualifiers
patients undergoing elective robot assisted hiatal hernia repair
Disqualifiers
patients less than 18 years of age
conversion to open surgery
BMI > 40
history of abdominoplasty
Trial design
Treatments tested in this trial
- Low pressure pneumoperitoneum (8-10mmHg) with AirSeal device
- Standard pressure pneumoperitoneum (13- 15 mmHg) with AirSeal device