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Clinical Trials/KCT0007445
KCT0007445
Not yet recruiting
未知

A clinical study on the efficacy of ultrasonic Energy Devices for Surgical Applications developed with Domestic technology in laparoscopic colorectal surgery.

Samsung Medical Center0 sites20 target enrollmentTBD
ConditionsNeoplasms

Overview

Phase
未知
Intervention
Not specified
Conditions
Neoplasms
Sponsor
Samsung Medical Center
Enrollment
20
Status
Not yet recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional Study
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • over 20 years old
  • A patient who was diagnosed with colorectal cancer as a result of a biopsy performed with a colonoscopy and is scheduled to undergo laparoscopic colorectal resection
  • Patients with ECOG (Estern Cooperative Oncology Group Performance Status) performance of 0 or 1
  • Patients who have not received chemotherapy or radiation therapy prior to surgery
  • Patients who did not take an anticoagulation agent/antiplatelet agent before surgery
  • Patients with diseases that are eligible for laparoscopic surgery
  • Patients who explained the study outline and, in principle, obtained informed consent (regulation form) from the patient himself/herself.
  • However, if it is necessary for patients over 70 years of age, ? the research subject understands information related to the research (eg, the nature of the research and expected research results), ? can logically handle the information about the research, and ? After confirming that they have the ability to clearly express their choice regarding whether or not they want to participate, if the subject's understanding and willingness to participate in the study are repeatedly confirmed, they should participate in the study. If necessary, also have appropriate safeguards, such as obtaining your consent with a family member or legal representative.

Exclusion Criteria

  • If the patient or guardian does not consent to this study
  • open surgery
  • In case of accompanying cancer other than colorectal cancer
  • When there are two or more cancerous lesions
  • If patient have received chemotherapy or radiation therapy before surgery
  • If distant metastasis is confirmed in preoperative examination
  • In case of metastatic colorectal cancer
  • If patient do not have the ability making decision
  • If patient is pregnant

Outcomes

Primary Outcomes

Not specified

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