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A prospective randomized trial comparing endoscopic stent placement with surgical gastrojejunostomy in gastric outlet obstruction caused by advanced gastric cancer

A prospective randomized trial comparing endoscopic stent placement with surgical gastrojejunostomy in gastric outlet obstruction caused by advanced gastric cancer - Surgical bypass vs endoscopic stent in malignant gastric outlet obstruction:a randomized trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000013883
Enrollment
120
Registered
2014-05-03
Start date
2014-02-13
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

gastric cancer

Interventions

gastrojejunal bypass endoscopic stent

Sponsors

Osaka University Graduate School of Medicine,Department of Gastroenterology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Gastric adenocarcinoma diagnosed by biopsy Un resectable cancer Gastric cancer which does not occur in residual stomach after surgery Patients who are not be able to take solid meal due to a stricture caused by tumor Patients who are assessed to be able to have the operations Blood test which is taken within 2 weeks before registration show following results; White blood cell count >3000/mm3 Hemoglobin level >7.0 g/dL Platelet count>100,000 /mm3 Serum total bilirubin level<3.0 mg/dL Serum creatinine level <2.0 mg/dL Performance status score 0-2 Patents with survival expectancy more than 3 months The enrollment in the study is confirmed in written consent

Exclusion criteria

Exclusion criteria: Cases of emergency operation for gastric perforation,bleeding or etc. Cases of simultaneous or recurrence of heterochronous active double cancer Patients with a history of or are suspected of brain metastasis or carcinomatous meningitis Patients with Disseminated Intravascular Coagulation Patients with mental disorder or abnormal mental status and are assessed to be difficult to join the study Patients with severe ascites Patients with a history of radiotherapy

Design outcomes

Primary

MeasureTime frame
Length of the period which oral intake is possible after the intervention

Secondary

MeasureTime frame
Safety of the procedure, Improvement of oral intake, Survival period after the procedure, Necessity of additional intervention, Length of the period which patient is able to stay home, Quality of life after the procedure

Countries

Japan

Contacts

Public ContactShuji Takiguchi

Osaka University Gastroenterological Sugery

stakiguchi@gesurg.med.osaka-u.ac.jp+81668793251

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026