The da Vinci Single Port Robotic System for Use in Abdominal and Pelvic Surgical Procedures
Recruiting
Phase 2
Interventional Study
Disease or Disorder
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Trial phase
- Phase 2
- Study type
- Interventional
- Purpose
- Device Feasibility
- Participants needed
- 33 (estimated)
- Sponsor
- City of Hope Medical Center · Other
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About This Trial
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…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Documented informed consent of the participant and/or legally authorized representative
* Any patient scheduled to undergo robot-assisted abdominal or pelvic procedures
* Age \> 18 years
Exclusion Criteria:
* Body mass index (BMI) \> 45
* Contraindications to minimally invas…
Contacts
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