Treatment Algorithm for Nausea and Vomiting in the Palliative Phase
Nausea, Vomiting, Cancer
About this trial
This is an interventional treatment trial for Nausea focused on measuring palliative care, palliative medicine, palliative
Eligibility Criteria
Inclusion Criteria:
- patients 18 years or older in the palliative phase and
- who suffer from nausea or vomiting with a rating on a numeric rating scale (NRS) of more than 2 and
- have a wish to be treated and
- where no treatable cause is assignable
Exclusion Criteria:
- Patients not able to sign informed consent.
- Patients with known contra-indications for metoclopramide, 5HT-3 antagonists or dexamethasone.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
algorithm 1 first metoclopramide
algorithm 2 first granisetron
metoclopramide 10 mg tablets 3x daily orally and in those patients that cannot swallow tablets the medication will be substituted by suppositories 10 mg 3x daily rectally. In case of failure, granisetron patch 3.1mg/24 hours will be added to the treatment and a loading dose of 2 mg granisetron oral if the patient can swallow. In case of toxicity metoclopramide will be stopped. In case of failure of the combination (second step) or toxicity, an oral dose of dexamethasone 8 mg will be added daily.
granisetron patch 3.1 mg/24 hours will be offered to the patient, and a loading dose of 2 mg granisetron oral if the patient can swallow In case of failure, metoclopramide 10 mg tablets 3x daily orally will be added and in those patients that cannot swallow tablets the oral medication will be substituted with rectal suppositories 10 mg. The granisetron patch will only be withdrawn from patients that suffer from clinically relevant toxicity. Metoclopramide will then be administered. In the case of secondary failure or toxicity, dexamethasone 8 mg orally daily will be added.