drugset / Trial / NCT00332696

Octreotide Compared to Placebo in Patients With Inoperable Bowel Obstruction Due to Peritoneal Carcinomatosis

NCT00332696

Phase 2 Completed 64 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupDouble-blindTreatment

Summary

To evaluate in combination with corticosteroid and local standard medical care the efficacy and safety of long-acting octreotide compared to placebo for the treatment of symptoms of inoperable bowel obstruction in patients with peritoneal carcinomatosis

Timeline

Start
2005-09
Primary completion
2008-09
Completion
2008-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Octreotide Peptide 0.1 mg/ml Intramuscular
Subject Octreotide Peptide 30 mg Intramuscular
Background Methylprednisolone Other / unclassified 3 mg/kg Intravenous
Background Methylprednisolone Other / unclassified 4 mg/kg Intravenous