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
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.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Chicago, Illinois, United States
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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