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NCT00287872 · OUTCOME

Peripheral Motor and Sensory Neuropathy (Grade 2 and Higher)

Bortezomib and Thalidomide in Treating Patients With Newly Diagnosed Stage II or Stage III Multiple Myeloma · Source last updated 2018-03-01

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

Measure
NUMBER
Unit
participants
Interval / dispersion
Not reported
Time frame
1-6 months

What was measured

Neuropathy was monitored using Total Neuropathy Score reduced (TNSr).

Groups in this outcome

Bortezomib and Thalidomide

The patients will receive Bortezomib on days 1, 4, 8 and 11 of each 21 day cycle in combination with daily oral Thalidomide. bortezomib thalidomide

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

Analysis denominator · Participants

GroupSource count
Bortezomib and Thalidomide27

Reported measurements

Source class 1
Values in participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Bortezomib and Thalidomide19Not reportedNot reportedNot reportedNot reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        value
        19
denoms
  1. counts
    1. group Id
      OG000
      value
      27
    units
    Participants
description
Neuropathy was monitored using Total Neuropathy Score reduced (TNSr).
groups
  1. description
    The patients will receive Bortezomib on days 1, 4, 8 and 11 of each 21 day cycle in combination with daily oral Thalidomide. bortezomib thalidomide
    id
    OG000
    title
    Bortezomib and Thalidomide
param Type
NUMBER
reporting Status
POSTED
time Frame
1-6 months
title
Peripheral Motor and Sensory Neuropathy (Grade 2 and Higher)
type
SECONDARY
unit Of Measure
participants

Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f

Preserved source evidence · Not medical advice