Malignant Gastric Outlet Obstruction Clinical Trial
— SEMSOfficial title:
The Usefulness of Self-expandable Metal Stents(SEMS) for Malignant Gastric Outlet Obstruction: a Prospective Study Using New Designed Stents
The purpose of this study is to evaluate usefulness of new designed winged stent(SEMS).
Status | Recruiting |
Enrollment | 33 |
Est. completion date | December 2015 |
Est. primary completion date | December 2015 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 19 Years and older |
Eligibility |
Inclusion Criteria: 1. Gastric outlet obstruction symptom 2. Diagnosis of gastric outlet obstruction by radiologist or endoscopist 3. Gastric outlet obstruction by malignant disease 4. Aged over 19 5. Informed consent Exclusion Criteria: 1. Gastric outlet obstruction by benign disease or infectious disease 2. Could not endoscopic intervention by poor general condition 3. Refusal of patient |
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Korea, Republic of | Asan Medical Center | Seoul | Songpa-gu |
Lead Sponsor | Collaborator |
---|---|
Asan Medical Center |
Korea, Republic of,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Complication rate(stent migration and tumor ingrowth) of new designed winged stent | It will be assessed by a composite measure consisting of physical exam, ECOG PS, GOOSS and gastrointestinal imaging. | up to 16 weeks from stent insertion | Yes |
Secondary | Evaluate the technical success rate of SEMS insertion | It will be assessed by a composite measure consisting of physical exam, ECOG PS, GOOSS and gastrointestinal imaging. | up to 16 weeks from stent insertion | No |
Secondary | Evaluate the clinical success rate of SEMS insertion | It will be assessed by a composite measure consisting of physical exam, ECOG PS, GOOSS and gastrointestinal imaging. | up to 16 weeks from stent insertion | No |
Secondary | Difference of insertion time between previous stent insertion and new designed stent | 1 years | No |
Status | Clinical Trial | Phase | |
---|---|---|---|
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