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UMCC 2008.048 Palonosetron for the Treatment of Nausea and Vomiting in Terminally Ill Patients (HUM21469)
The primary objective of this study is to determine the complete response (no vomiting and no need for other medications to treat nausea) in terminally ill patients suffering from nausea and/or vomiting, who are treated with palonosetron. Another objective is to determine the partial response (relief of nausea and vomiting to the extent that the patient wishes to continue treatment with palonosetron) after being treated with palonosetron. Palonosetron is currently approved by the FDA to prevent nausea and vomiting associated with chemotherapy. The investigators are testing this medication to see if it can help to relieve nausea and vomiting not associated with chemotherapy.
Details
| Lead sponsor | University of Michigan Rogel Cancer Center |
|---|---|
| Phase | Phase 2 |
| Status | TERMINATED |
| Enrolment | 3 |
| Start date | 2010-11 |
| Completion | 2013-05 |
Conditions
- Nausea
- Vomiting
- Terminally Ill
Interventions
- Palonosetron
Primary outcomes
- To Determine the Complete Response (no Vomiting and no Need for Nausea Rescue Medication) in Terminally Ill Patients Suffering From Nausea and/or Vomiting, Treated With Palonosetron. — 96 hours after dosing
Countries
United States