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NCT02739594 · OUTCOME

Number of Zoledronate Dose Reductions for Each Participant

Comparison of Ibandronate - Zoledronate Regarding Nephrotoxicity in Multiple Myeloma · Source last updated 2016-07-22

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

Measure
MEAN
Unit
dose reductions
Interval / dispersion
Standard Deviation
Time frame
From Baseline to end of study (up to Week 96)

What was measured

The number of zoledronate dose reductions was averaged across all participants, including those participants who did not have any dose reductions during the study.

Analysis population: ITT Population; only the Zoledronate arm was included.

Groups in this outcome

Zoledronate

Participants with multiple myeloma received zoledronate via 15-minute IV infusion as 4 mg every 4 weeks for up to 92 weeks. As a result of slow recruitment, the treatment duration was shortened to 40 weeks for participants who had not yet received 48 weeks of treatment. All participants returned for an additional follow-up observation 4 weeks after the end of treatment.

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

Analysis denominator · Participants

GroupSource count
Zoledronate40

Reported measurements

Source class 1
Values in dose reductions · Interval/dispersion: Standard Deviation
GroupValueSpreadLowerUpperComment
Zoledronate0.81.4Not reportedNot reportedNot reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        spread
        1.4
        value
        0.8
denoms
  1. counts
    1. group Id
      OG000
      value
      40
    units
    Participants
description
The number of zoledronate dose reductions was averaged across all participants, including those participants who did not have any dose reductions during the study.
dispersion Type
Standard Deviation
groups
  1. description
    Participants with multiple myeloma received zoledronate via 15-minute IV infusion as 4 mg every 4 weeks for up to 92 weeks. As a result of slow recruitment, the treatment duration was shortened to 40 weeks for participants who had not yet received 48 weeks of treatment. All participants returned for an additional follow-up observation 4 weeks after the end of treatment.
    id
    OG000
    title
    Zoledronate
param Type
MEAN
population Description
ITT Population; only the Zoledronate arm was included.
reporting Status
POSTED
time Frame
From Baseline to end of study (up to Week 96)
title
Number of Zoledronate Dose Reductions for Each Participant
type
SECONDARY
unit Of Measure
dose reductions

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

Preserved source evidence · Not medical advice