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NCT05672368

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

Recruiting now Phase 2 Last updated 1 May 2025
What this trial tests

Phase 2 trial testing Robot-Assisted Surgery in Disease or Disorder in 33 participants. Currently enrolling.

Timeline
26 April 2024
Primary endpoint
27 January 2026
27 January 2026

Quick facts

Lead sponsorCity of Hope Medical Center
PhasePhase 2
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposedevice feasibility
Enrollment33
Start date26 April 2024
Primary completion27 January 2026
Estimated completion27 January 2026
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

City of Hope Medical Center

Who can join

18 and older, any sex, with Disease or Disorder. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other City of Hope Medical Center trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05672368.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing