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Not Yet Recruiting NCT05672368

The da Vinci Single Port Robotic System for Use in Abdominal and Pelvic Surgical Procedures

Conditions: Disease or Disorder

Sex: All
Ages: 18 Years – N/A
Phase: PHASE2
Enrollment: 33
Sponsor: City of Hope Medical Center

Location: United States

Summary

This phase II trial test the effectiveness and safety of a single-port robotic device (the da Vinci single port [SP]1098) for use in abdominal and pelvic surgeries. The da Vinci SP1098 robotic device can be used to perform less invasive surgeries that allow entry into the body through a single, small incision. The use of this device during surgery may allow surgeons to perform complex procedures that result in less pain, fewer complications and side effects, and improved recovery.

Eligibility Criteria

Inclusion Criteria:Documented informed consent of the participant and/or legally authorized representativeAny patient scheduled to undergo robot-assisted abdominal or pelvic proceduresAge > 18 yearsExclusion Criteria:Body mass index (BMI) > 45Contraindications to minimally invasive surgery including chronic obstructive pulmonary disordersPast history of failed attempt of minimally invasive abdominal or pelvic surgery

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05672368). StuddyBuddy aggregates publicly available trial information.