KCT0005989
Recruiting
N/A
A prospective study for evaluation of efficacy of a 12mm diameter polytetrafluoroethylene partial covered stent in malignant extrahepatic biliary obstruction
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Asan Medical Center
- Enrollment
- 161
- Status
- Recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\) Adult patients aged 19 to under 80 years of age
- •2\) Patients who are closed to malignancy, which is not surgical or resectable
- •3\) Patients with obstructive obstruction caused by lymph node metastasis in the primary carcinoma other than the liver
- •4\) Patients who cannot or fail endoscopic stent implantation
- •5\) Patients who have not previously undergone bile duct surgery
- •6\) Patients with an expected survival rate of at least 2 months (Eastern Cooperative Oncology Group Performance Status \[ECOG\-PS] less than 3 points)
Exclusion Criteria
- •1\) Patients who had previously undergone endoscopic stent implantation or bile duct surgery
- •2\) Patients with expansion of biliary tract in the liver or external biliary tract in the liver
- •3\) Hemophilia patients
- •4\) Patients with three or more ECOG points
Outcomes
Primary Outcomes
Not specified
Similar Trials
Active, Not Recruiting
Phase 1
A prospective study to assess the effectiveness of lignocaine versus normal saline in the reduction of pain associated with dressing removal in finger tip injuriesFinger tip injuriesEUCTR2005-005591-32-GBDerby Hospitals NHS Foundation Trust20
Completed
N/A
A prospective study to assess the effectiveness of lignocaine versus normal saline in the reduction of pain associated with dressing removal in fingertip injuriesISRCTN59113767Record Provided by the NHSTCT Register - 2007 Update - Department of Health98
Not Yet Recruiting
Phase 4
Steroid injections or Rebamipide tablets, which is better to treat painful and difficult mouth opening (OSMF)Health Condition 1: K135- Oral submucous fibrosisCTRI/2022/12/048127Osmania Medical College
Completed
Phase 1
A prospective study to investigate the efficacy of cytoreductive surgery combined with perioperative intraperitoneal chemotherapy for pseudomyxoma peritoneipseudomyxoma peritoneiJPRN-UMIN000011384ational Center for Global Health and Medicine75
Completed
N/A
The prospective study to evaluate the efficacy of the combination therapy of inhaled budesonide/formoterol fumarate, clarithromycin, and montelukast in AFO after allogeneic SCTAir flow obstruction after allogeneic SCTJPRN-UMIN000022048Department of Hematology, Chiba University Hospital85