2 studies in Symptom Management
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Effectiveness of Aprepitant in Addition to Ondansetron in the Prevention of Nausea and Vomiting Caused by Upper Abdominal Radiotherapy
Scottsdale and Phoenix, AZ
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Effectiveness of Aprepitant in Addition to Ondansetron in the Prevention of Nausea and Vomiting Caused by Upper Abdominal Radiotherapy
Location:
Scottsdale and Phoenix, AZTrial status:
Open for EnrollmentWhy is this study being done?
Severe nausea and/or vomiting in patients receiving radiotherapy to the upper abdomen is common despite having received pre-medication with ondansetron, a standard preventive treatment. This study aims to reduce the incidence of significant nausea and/or vomiting with the addition of the NK1-antagonist aprepitant to standard ondansetron treatment. This study will also assess the safety and tolerability of prolonged administration of aprepitant over the 4 to 6 week period of radiation treatment.
NCT ID:
NCT00970905IRB Number:
10-002651Who can I contact for additional information about this study?
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Scottsdale: Clinical Trials Referral Office 507-538-7623
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EUS Guided Celiac Neurolysis
Rochester, MN
View Summary
EUS Guided Celiac Neurolysis
Location:
Rochester, MNTrial status:
Open for EnrollmentWhy is this study being done?
- Hypothesis: - Direct CGN enhances neurolytic drug delivery into celiac ganglia and increases the efficacy of neurolysis and subsequent pain control and survival in patients with pancreatic carcinoma. - Rationale: - Standard CPN leads to inaccurate delivery of the injectate with rapid dispersal thereby only briefly remaining in contact with neural structures and limiting the degree of neurolysis. Poor targeting and delivery of a neurolytic agent may result in diminished neurolysis and decrease efficacy.
NCT ID:
NCT01615653IRB Number:
09-005037Who can I contact for additional information about this study?
Rochester: Michael J Levy, MD 507-266-6931
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