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Treatment Algorithm for Nausea and Vomiting in the Palliative Phase

Primary Purpose

Nausea, Vomiting, Cancer

Status
Unknown status
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
metoclopramide
granisetron
Dexamethasone
Granisetron 2Mg Tablet
Sponsored by
Radboud University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Nausea focused on measuring palliative care, palliative medicine, palliative

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

    Arm Type

    Active Comparator

    Active Comparator

    Arm Label

    algorithm 1 first metoclopramide

    algorithm 2 first granisetron

    Arm Description

    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 The granisetron patch will only be withdrawn from patients that suffer from clinically relevant toxicity.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.

    Outcomes

    Primary Outcome Measures

    NRS nausea
    response defined as NRS <3 or decrease of more than 2 on NRS and absence of vomiting or retching in the last 3 days

    Secondary Outcome Measures

    days from T0 to control
    The time from T0 until the moment that nausea and vomiting/retching is in control

    Full Information

    First Posted
    April 21, 2016
    Last Updated
    January 9, 2017
    Sponsor
    Radboud University Medical Center
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03017391
    Brief Title
    Treatment Algorithm for Nausea and Vomiting in the Palliative Phase
    Official Title
    Feasibility Study to Compare 2 Strategies of Treatment Algorithm for Treating Nausea and or Vomiting in the Palliative Phase of Cancer Care
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    December 2016
    Overall Recruitment Status
    Unknown status
    Study Start Date
    January 2017 (undefined)
    Primary Completion Date
    April 2018 (Anticipated)
    Study Completion Date
    undefined (undefined)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Radboud University Medical Center

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Nausea and vomiting are frequently occurring problems in the palliative phase of patients with cancer. Between 20-50% of them regularly suffer from nausea, retching or vomiting. Often the cause of nausea and vomiting is multifactorial and symptomatic treatment is necessary. Potential drugs for symptomatic anti-nausea therapy are metoclopramide, serotonin antagonists, the combination of both and dexamethasone as rescue medication in case of failure. There is no data that depicts which strategy is the best. This study will be conducted to unravel which treatment algorithm is most successful.
    Detailed Description
    Nausea and vomiting are frequently occurring problems in the palliative phase of patients with cancer. Between 20-50% of them regularly suffer from nausea, retching or vomiting. Often the cause of nausea and vomiting is multifactorial and symptomatic treatment is necessary. Potential drugs for symptomatic anti-nausea therapy are metoclopramide, serotonin antagonists, the combination of both and dexamethasone as rescue medication in case of failure. There is no data that depicts which strategy is the best. This study will be conducted to unravel which treatment algorithm is most successful: 1 to start with metoclopramide, to add a serotonin antagonist (granisetron transdermal patch and 2 milligram granisetron oral loading dose if the patient can swallow) in case of failure and to add dexamethasone as rescue medication versus 2 an algorithm to start with a serotonin antagonist (granisetron transdermal patch and 2 milligram granisetron oral loading dose if the patient can swallow), to add metoclopramide in case of failure and to add dexamethasone as rescue medication. Granisetron plaster is a new formulation of a well known serotonin antagonist and might be useful especially within the patient group in the palliative phase. The questions are: Is it feasible to compare treatment algorithms for symptomatic treatment of nausea and vomiting in palliative cancer patients? And is a stepwise symptomatic treatment algorithm to manage nausea and vomiting using metoclopramide or granisetron transdermal patch as a start medication effective in palliative patients in at least one of both treatment arms? Patients will be asked to complete the QLQC30 and ESAS on different moments during the study. Besides, they will be asked to complete a diary for nausea severity (NRS scale 0-10) and for the frequency of vomiting and retching twice daily. Success of a treatment algorithm is defined as nausea is < 3 on NRS or a decrease of >2 on NRS for nausea combined with an absence of vomiting or retching in the last 3 days. Incomplete success is defined as nausea of 3 on NRS during one occasion of the last 3 days before the end of study but less than 4, no more than one retching a day during that period and absence of vomiting. Complete failure is defined as nausea of 4 or more on an NRS during the last 3 days or more than one retching daily or any vomiting or in case the patient has stopped all medication due to side effects.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Nausea, Vomiting, Cancer
    Keywords
    palliative care, palliative medicine, palliative

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 4
    Interventional Study Model
    Crossover Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    20 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    algorithm 1 first metoclopramide
    Arm Type
    Active Comparator
    Arm Description
    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.
    Arm Title
    algorithm 2 first granisetron
    Arm Type
    Active Comparator
    Arm Description
    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.
    Intervention Type
    Drug
    Intervention Name(s)
    metoclopramide
    Intervention Description
    metoclopramide 10 mg tablets 3x daily orally or suppositories 10 mg 3x daily rectally, use until toxicity
    Intervention Type
    Drug
    Intervention Name(s)
    granisetron
    Other Intervention Name(s)
    Sancuso
    Intervention Description
    granisetron patch 3.1mg/24 hours, use until toxicity
    Intervention Type
    Drug
    Intervention Name(s)
    Dexamethasone
    Intervention Description
    dexamethasone 8 mg, last step in both algorithms
    Intervention Type
    Drug
    Intervention Name(s)
    Granisetron 2Mg Tablet
    Intervention Description
    granisetron 2 mg loading dose
    Primary Outcome Measure Information:
    Title
    NRS nausea
    Description
    response defined as NRS <3 or decrease of more than 2 on NRS and absence of vomiting or retching in the last 3 days
    Time Frame
    15 days
    Secondary Outcome Measure Information:
    Title
    days from T0 to control
    Description
    The time from T0 until the moment that nausea and vomiting/retching is in control
    Time Frame
    two weeks
    Other Pre-specified Outcome Measures:
    Title
    feasibility
    Description
    number of included patients a 6 months period
    Time Frame
    6 months
    Title
    comparison of starting metoclopramide to starting with granisetron
    Description
    response defined as NRS <3 or decrease of more than 2 on NRS and absence of vomiting or retching in the last 3 days
    Time Frame
    6 months
    Title
    quality of life
    Description
    QLQC30 scale
    Time Frame
    15 days
    Title
    adverse events
    Description
    diary adverse events
    Time Frame
    14/15 days

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    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.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Christa v Schaik
    Phone
    024-3610353
    Email
    christa.vanschaik@radboudumc.nl
    First Name & Middle Initial & Last Name or Official Title & Degree
    C.A.H.H.V.M. Verhagen, M.D. Ph.D.
    Phone
    024-3610353
    Email
    Stans.verhagen@radboudumc.nl
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    C.A.H.H.V.M. Verhagen, M.D. Ph.D.
    Organizational Affiliation
    Radboud University Medical Center
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    Treatment Algorithm for Nausea and Vomiting in the Palliative Phase

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