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Search / Trial NCT00004910

Endoscopic Placement of Metal Stents in Treating Patients With Cancer- Related Duodenal Obstruction

Launched by NORTHWESTERN UNIVERSITY · May 8, 2003

Trial Information

Current as of August 11, 2025

Completed

Keywords

Stage I Colon Cancer Stage Ii Colon Cancer Stage Iii Colon Cancer Stage Iv Colon Cancer Stage I Gastric Cancer Stage Ii Gastric Cancer Stage Iii Gastric Cancer Stage Iv Gastric Cancer Recurrent Gastric Cancer Stage I Pancreatic Cancer Stage Ii Pancreatic Cancer Stage Iii Pancreatic Cancer Recurrent Pancreatic Cancer Recurrent Colon Cancer Localized Gastrointestinal Carcinoid Tumor Regional Gastrointestinal Carcinoid Tumor Metastatic Gastrointestinal Carcinoid Tumor Recurrent Gastrointestinal Carcinoid Tumor Small Intestine Adenocarcinoma Small Intestine Lymphoma Small Intestine Leiomyosarcoma Localized Extrahepatic Bile Duct Cancer Unresectable Extrahepatic Bile Duct Cancer Recurrent Extrahepatic Bile Duct Cancer Recurrent Small Intestine Cancer Constipation, Impaction, And Bowel Obstruction Quality Of Life Gastrointestinal Stromal Tumor Stage Iv Pancreatic Cancer

ClinConnect Summary

OBJECTIVES:

* Determine the objective response and clinical outcome in patients with duodenal obstruction secondary to malignancy treated with enteral Wallstents.
* Evaluate the efficacy and safety of this treatment in these patients.
* Evaluate the quality of life of these patients after enteral Wallstent placement.

OUTLINE: Patients undergo enteral Wallstent placement through an endoscope under fluoroscopic guidance into the duodenum.

Quality of life is assessed at 48 hours and 6 months after procedure.

Patients are followed at 48 hours, 30 days, 6 months, and then yearly thereafter u...

Gender

ALL

Eligibility criteria

  • DISEASE CHARACTERISTICS:
  • Endoscopically confirmed localized tumor as the cause of duodenal obstruction
  • All primary tumor types are eligible
  • No prior duodenal Wallstents
  • * Must have symptoms of gastrointestinal obstruction, including:
  • Inability to move bowels, absence of flatus, nausea/vomiting, abdominal pain, or diarrhea
  • PATIENT CHARACTERISTICS:
  • Age:
  • 18 and over
  • Performance status:
  • ECOG 0-3
  • Life expectancy:
  • Not specified
  • Hematopoietic:
  • Platelet count greater than 50,000/mm\^3
  • Hepatic:
  • INR no greater than 1.5 times upper limit of normal
  • Renal:
  • Not specified
  • Cardiovascular:
  • No cardiac condition
  • Other:
  • Not pregnant or nursing
  • Fertile patients must use effective contraception
  • No significant active infection (e.g., pneumonia, peritonitis, or wound abscess) that would preclude endoscopy
  • No other serious concurrent illness
  • No uncontrolled metabolic disease (e.g., diabetes mellitus or hypothyroidism)
  • No dementia, psychiatric disorder, or altered mental status that would preclude compliance
  • History of other neoplastic disease allowed
  • Veterans Administration patients are not eligible
  • PRIOR CONCURRENT THERAPY:
  • Biologic therapy:
  • Not specified
  • Chemotherapy:
  • Prior or concurrent chemotherapy allowed
  • Endocrine therapy:
  • Not specified
  • Radiotherapy:
  • Prior or concurrent radiotherapy allowed
  • Surgery:
  • At least 3 weeks since prior surgery and recovered

About Northwestern University

Northwestern University is a prestigious academic institution renowned for its commitment to advancing medical research and improving patient care through innovative clinical trials. With a robust infrastructure that supports interdisciplinary collaboration, Northwestern leverages its expertise in various fields, including medicine, engineering, and social sciences, to drive groundbreaking studies. The university is dedicated to adhering to the highest ethical standards and regulatory compliance, ensuring that all clinical trials are conducted with the utmost integrity and focus on participant safety. Through its Clinical Trials Office, Northwestern aims to translate scientific discoveries into effective therapies, ultimately enhancing health outcomes and contributing to the broader medical community.

Locations

Chicago, Illinois, United States

Patients applied

0 patients applied

Trial Officials

Willis G. Parsons, MD, PC

Study Chair

Robert H. Lurie Cancer Center

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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