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NCT00183820 · OUTCOME

Overall Survival

Study of Gemcitabine, Oxaliplatin, and Paclitaxel in Patients With Refractory Germ Cell Carcinoma · Source last updated 2026-07-01

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

Measure
MEDIAN
Unit
Months
Interval / dispersion
95% Confidence Interval
Time frame
Through study completion, about 9 years

What was measured

Measuring Overall Survival

Groups in this outcome

Paclitaxel, Gemcitabine, and Oxaliplatin

paclitaxel, gemcitabine, and oxaliplatin: 1. Paclitaxel 170 mg/m2 IV d 1 14 days 2. Gemcitabine 800 mg/m2 IV d 1 14 days 3. Oxaliplatin 100 mg/m2 IV d 1 14 days

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

Analysis denominator · Participants

GroupSource count
Paclitaxel, Gemcitabine, and Oxaliplatin30

Reported measurements

Source class 1
Values in Months · Interval/dispersion: 95% Confidence Interval
GroupValueSpreadLowerUpperComment
Paclitaxel, Gemcitabine, and Oxaliplatin18.3Not reported12.071.8Not reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        lower Limit
        12.0
        upper Limit
        71.8
        value
        18.3
denoms
  1. counts
    1. group Id
      OG000
      value
      30
    units
    Participants
description
Measuring Overall Survival
dispersion Type
95% Confidence Interval
groups
  1. description
    paclitaxel, gemcitabine, and oxaliplatin: 1. Paclitaxel 170 mg/m2 IV d 1 14 days 2. Gemcitabine 800 mg/m2 IV d 1 14 days 3. Oxaliplatin 100 mg/m2 IV d 1 14 days
    id
    OG000
    title
    Paclitaxel, Gemcitabine, and Oxaliplatin
param Type
MEDIAN
reporting Status
POSTED
time Frame
Through study completion, about 9 years
title
Overall Survival
type
SECONDARY
unit Of Measure
Months

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

Preserved source evidence · Not medical advice