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RECRUITING NA

Evaluation of SINGLE PORT (SP) Robotic Technology in Colorectal Surgery

NCT05321134 · View on ClinicalTrials.gov ↗

Study Summary

Currently a multiport robotic surgery platform (Intuitive Xi) is widely available and used for colorectal surgery indications. A Single port platform (Intuitive SP) is FDA approved for Head and Neck and Urology but has not been widely used in colorectal surgery. This study seeks to evaluate the safe and effective use of the SP platform for colorectal surgery indications.

Interventions

  • DEVICE Single port robotic colorectal surgical procedure

Study Locations (1)

California

  • UC Davis Medical Center — Sacramento

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2022-04-28
Est. Completion 2028-04
Phase NA

Sponsor

University of California, Davis

653 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05321134

The ClinicalTrials.gov registry entry for NCT05321134 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 25 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of California, Davis, which has 653 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 4 conditions, with Colo-rectal Cancer appearing as the primary indexed condition, and to 1 intervention — of which Single port robotic colorectal surgical procedure is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05321134 reports 1 study location spanning 1 distinct geographic area — top geographies include California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05321134 about?

NCT05321134 is a clinical study titled "Evaluation of SINGLE PORT (SP) Robotic Technology in Colorectal Surgery". Currently a multiport robotic surgery platform (Intuitive Xi) is widely available and used for colorectal surgery indications. A Single port platform (Intuitive SP) is FDA approved for Head and Neck and Urology but has not been widely used in colorectal surgery. This study seeks to evaluate the safe...

What is the current status of trial NCT05321134?

This trial is currently recruiting. It is a NA study. The enrollment target is 25 participants. The study started on 2022-04-28. Estimated completion is 2028-04.

What conditions does trial NCT05321134 study?

This clinical trial studies the following conditions: Colo-rectal Cancer, Colorectal Disorders, Rectal Prolapse, Colostomy Stoma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05321134?

The interventions under investigation include: Single port robotic colorectal surgical procedure (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05321134?

This trial is sponsored by University of California, Davis, which has 653 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05321134 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial