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NCT00346164 · OUTCOME

Toxicity Rate

Observation, Radiation Therapy, Combination Chemotherapy, and/or Surgery in Treating Young Patients With Soft Tissue Sarcoma · Source last updated 2022-04-28

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

Measure
NUMBER
Unit
percentage of participants
Interval / dispersion
95% Confidence Interval
Time frame
13 weeks

What was measured

Percentage of Arm D patients experiencing grade 4+ adverse events.

Analysis population: Excluding ineligible patients and patients not treated based on the protocol.

Groups in this outcome

Arm D

Intermediate \& High Risk; Neoadjuvant chemoradiotherapy

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

Analysis denominator · Participants

GroupSource count
Arm D196

Reported measurements

Source class 1
Values in percentage of participants · Interval/dispersion: 95% Confidence Interval
GroupValueSpreadLowerUpperComment
Arm D3.06Not reported0.655.47Not reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        lower Limit
        0.65
        upper Limit
        5.47
        value
        3.06
denoms
  1. counts
    1. group Id
      OG000
      value
      196
    units
    Participants
description
Percentage of Arm D patients experiencing grade 4+ adverse events.
dispersion Type
95% Confidence Interval
groups
  1. description
    Intermediate \& High Risk; Neoadjuvant chemoradiotherapy
    id
    OG000
    title
    Arm D
param Type
NUMBER
population Description
Excluding ineligible patients and patients not treated based on the protocol.
reporting Status
POSTED
time Frame
13 weeks
title
Toxicity Rate
type
SECONDARY
unit Of Measure
percentage of participants

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

Preserved source evidence · Not medical advice