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Image-guided Minimally Invasive Robotic Surgery Using Preoperative CT Scan for Gastric Cancer Patients

A Feasibility Study on Image-guided Minimally Invasive Robotic Surgery Using Preoperative CT Scan for Gastric Cancer Patients

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01338948
Enrollment
12
Registered
2011-04-20
Start date
2009-08-31
Completion date
2009-12-31
Last updated
2011-04-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gastric Cancer

Brief summary

The purpose of this study is to assess the feasibility of image-guided surgery in patients with early stage gastric cancer using Robotic Surgery with Tile-pro program. For the assessment of the feasibility, conversion to open or laparoscopic surgery due to disturbance of will indicate the failure.

Detailed description

To assess the feasibility of image-guided surgery in patients with early stage gastric cancer using Robotic Surgery with Tile-pro program. For the assessment of the feasibility, conversion to open or laparoscopic surgery due to disturbance of will indicate the failure. Diagnosis of early stage gastric cancer -\> CT scanning & EUS for staging -\> (Registration) -\> Robotic surgery with image reconstruction -\> Conversion rate, Tumor location & vascular anatomy correlation.

Interventions

PROCEDUREpreoperative 3D-CT reconstruction

Robotic Surgery with CT reconstruction images using Tile-pro program.

Sponsors

Yonsei University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients who are older than 20 years * Histologically confirmed gastric adenocarcinoma * Patients who want robotic gastric cancer surgery * Preoperative clinical stage Stage I (T1N0, T1N1, T2N0) diagnosed with EGD, EUS & CT scan * No history of drug allergy * creatinine \< 1.5 X upper normal limit * Informed consent

Exclusion criteria

* Previous history of upper abdominal surgery * Patient refused the study

Design outcomes

Primary

MeasureTime frameDescription
rate of conversion (to laparotomy or laparoscopy assisted)within 24 hours after operationVisualization of upper abdominal vessels (seven vascular structures encountered during gastrectomy)

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 24, 2026