Expired Study
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Chicago, Illinois 60611


Purpose:

RATIONALE: Palliative therapy with octreotide may help patients who have bowel obstruction that cannot be removed by surgery to live longer and more comfortably. PURPOSE: Phase II trial to study the effectiveness of octreotide as palliative therapy in treating patients who have cancer-related bowel obstruction that cannot be removed by surgery.


Study summary:

OBJECTIVES: - Determine the effectiveness of octreotide in the palliation of bowel obstruction secondary to cancer. - Characterize the dose and tolerability of octreotide in this patient population. OUTLINE: Patients receive octreotide subcutaneously or IV over 24 hours on days 2-5. Patients who respond well to study may continue octreotide for palliative effects. PROJECTED ACCRUAL: A total of 9-25 patients will be accrued for this study over 9 months.


Criteria:

DISEASE CHARACTERISTICS: - Inoperable bowel obstruction secondary to cancer OR - Metastatic or primary abdominal cancer - Patient presents with vomiting - Percutaneous gastrostomy tube allowed PATIENT CHARACTERISTICS: Age: - Over 18 Performance status: - ECOG 0-4 Life expectancy: - Not specified Hematopoietic: - Not specified Hepatic: - Not specified Renal: - Not specified Other: - No documented hypersensitivity to octreotide - Not pregnant or nursing PRIOR CONCURRENT THERAPY: Biologic therapy: - Not specified Chemotherapy: - Prior chemotherapy allowed Endocrine therapy: - Concurrent steroids allowed Radiotherapy: - Prior radiotherapy allowed Surgery: - Not specified


NCT ID:

NCT00004895


Primary Contact:

Study Chair
J. Cameron Muir, MD
Robert H. Lurie Cancer Center


Backup Contact:

N/A


Location Contact:

Chicago, Illinois 60611
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: September 25, 2017

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