A randomised double blind placebo controlled trial of infusional subcutaneous octreotide in the management of malignant bowel obstruction at the end of life.
A randomised double blind placebo controlled trial of infusional subcutaneous octreotide in the management of malignant bowel obstruction in people with advanced cancer.
Flinders University
92 participants
Aug 22, 2008
Interventional
Conditions
Summary
This study looks at the effectiveness of the drug octreotide in palliative care management of bowel obstruction caused by cancer in people with advanced cancer. Who is it for? You can join this study if you have widespread and advanced cancer and you have a related bowel obstruction which requires hospital admission or a change in care if you are already in hospital, but surgical removal is not currently considered appropriate. Trial details Participants will be randomly divided into two groups. One group will receive a continuous infusion of the drugs octreotide and ranitidine under the skin (subcutaneous) in addition to intravenous doses of dexamethasone and intravenous or subcutaneous fluids for 72 hours. The other group (control) will receive fluids under the skin only. Bowel obstruction is a common medical problem in people with advanced cancer. Current treatment options include combinations of surgery (where this is possible), nil by mouth, a feeding tube placed into the stomach, pain relief, and medications that reduce secretions. None of these options has been tested in a study that is large enough to determine which works best. Octreotide can inhibit the release of hormones that cause secretions into the gut that may make the pain of bowel obstruction worse. Inhibiting these secretions with Octreotide may help relieve pain and improve the quality of life.
Eligibility
Plain Language Summary
Simplified for easier understanding
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
Interested in this trial?
Get notified about updates and connect with the research team.
Interventions
A phase III randomised, double blind, placebo controlled trial of octreotide (600mcg) delivered by continuous subcutaneous infusion used in conjunction with bolus daily parenteral (subcutaneous or intravenous) dexamethasone (8mg), ranitidine (200mg per 24 hours, either as bolus or continuous subcutaneous infusion) and parenteral hydration (continous subcutaneous or intravenous infusion) of(10mls/kg/24hours) over a maximum of 72 hours.
Locations(1)
View Full Details on ANZCTR
For the most up-to-date information, visit the official listing.
ACTRN12608000211369