Low Pressure Pneumoperitoneum Using AirSeal® for Reduction in Postoperative Shoulder Pain Following Robot Assisted Hiatal Hernia Repair

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorRiverside University Health System Medical Center

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

Treatment groups

120 Participants
are divided into 2 treatment groups