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Clinical Trials/KCT0002467
KCT0002467
Recruiting
未知

EUS guided RFA for the management of pancreatic and peripancreatic tumor; efficacy and safety evaluation

Asan Medical Center0 sites25 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Diseases of the digestive system
Sponsor
Asan Medical Center
Enrollment
25
Status
Recruiting
Last Updated
7 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\. Persons who are able to understand clinical trials of Adults under the age of 20 and under 80 years old who are voluntarily agreed to participate in this clinical trial, voluntarily agreeing to sign consent for this clinical trial.
  • 2\. Patients who have been diagnosed with tumors of pancreas and pancreatic tumors using biopsy.
  • 3\. Estimated expectation period of 6 months or more.
  • 4\. Patients who are inoperable and can not be Received radiation therapy due to a lack of immunity.
  • 5\. Patients who do not respond to existing anti\-cancer drugs and radiation therapy
  • 6\. cancer patient is examined by CT or MRI
  • 7\. Patients with \= 50 % of Karnofsky performance status
  • 8\. Patient whose results are normal in the blood coagulation test
  • 9\. Female of child bearing age must have negative results in pregnancy examinations..
  • 10\. Patients who follow the clinical trial procedure and comply with the visit schedule.

Exclusion Criteria

  • 1\. Patient who can not see images of endoscopic ultrasonography.
  • 2\. Patients with an obstruction in the endoscopy path
  • 3\. disseminated intravascular coagulation
  • 4\. Patients who are taking drugs that can cause bleeding, such as aspirin..
  • 5\. Chronic obstructive or restrictive chronic lung disease, including breathing difficulty during recess
  • 6\. Other serious diseases or medical conditions.
  • 7\. Pregnant women, breastfeeding women, and women of child bearing age who don't use proper contraception.
  • 8\. Other medical condition that may impair the ability of patients to participate in clinical trials.
  • 9\. Patients with significant neurologic or psychiatric disorder, such as dementia or strokes.
  • 10\. Despite the treatment unstable heart disease, a heart attack occurs within six months prior to the clinical trial (Even if a heart attack is diagnosed within six months prior to the clinical trial, a heart condition that remains stable is possible for enroll the study.)

Outcomes

Primary Outcomes

Not specified

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