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NCT02517021 · OUTCOME

Percentage of Patients With no Emetic Episodes in the Acute Phase

A Safety Study of Intravenous Pro-Netupitant and Palonosetron Combination for the Prevention of Nausea and Vomiting · Source last updated 2018-06-20

Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.

Measure
COUNT_OF_PARTICIPANTS
Unit
Participants
Interval / dispersion
Not reported
Time frame
0-24 hours

Groups in this outcome

Pro-netupitant/Palonosetron Plus Dexamethasone

Intravenous Pro-netupitant/Palonosetron (260 mg/0.25 mg) powder for solution for infusion (on Day 1) with oral dexamethasone prior to each scheduled chemotherapy cycle Pro-netupitant/Palonosetron Dexamethasone

Netupitant/Palonosetron Plus Dexamethasone

Oral netupitant/palonosetron (300 mg/0.50 mg) hard capsule (on Day 1) with oral dexamethasone prior to each scheduled chemotherapy cycle Netupitant/Palonosetron Dexamethasone

Group identifiers and denominators belong to this outcome only. They may differ in another outcome or in safety reporting.

Analysis denominator · Participants

GroupSource count
Pro-netupitant/Palonosetron Plus Dexamethasone203
Netupitant/Palonosetron Plus Dexamethasone201

Reported measurements

Source class 1
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Pro-netupitant/Palonosetron Plus Dexamethasone164Not reportedNot reportedNot reportedNot reported
Netupitant/Palonosetron Plus Dexamethasone165Not reportedNot reportedNot reportedNot reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        value
        164
      2. group Id
        OG001
        value
        165
denoms
  1. counts
    1. group Id
      OG000
      value
      203
    2. group Id
      OG001
      value
      201
    units
    Participants
groups
  1. description
    Intravenous Pro-netupitant/Palonosetron (260 mg/0.25 mg) powder for solution for infusion (on Day 1) with oral dexamethasone prior to each scheduled chemotherapy cycle Pro-netupitant/Palonosetron Dexamethasone
    id
    OG000
    title
    Pro-netupitant/Palonosetron Plus Dexamethasone
  2. description
    Oral netupitant/palonosetron (300 mg/0.50 mg) hard capsule (on Day 1) with oral dexamethasone prior to each scheduled chemotherapy cycle Netupitant/Palonosetron Dexamethasone
    id
    OG001
    title
    Netupitant/Palonosetron Plus Dexamethasone
param Type
COUNT_OF_PARTICIPANTS
reporting Status
POSTED
time Frame
0-24 hours
title
Percentage of Patients With no Emetic Episodes in the Acute Phase
type
SECONDARY
unit Of Measure
Participants

Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0

Preserved source evidence · Not medical advice