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NCT00676806 · OUTCOME

Compare Rates of Complications Between Patients Receiving Ablative vs. Non-myeloablative Conditioning Prior to UCB Transplantation

A Phase II Study of Umbilical Cord Blood Transplantation · Source last updated 2017-06-01

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

Measure
NUMBER
Unit
events
Interval / dispersion
Not reported
Time frame
+180 days

What was measured

Composite endpoint of GVH or infection. Too few events to compare between arms.

Groups in this outcome

Myeloablative Conditioning

Patients receiving umbilical cord blood for hematopoietic rescue following myeloablative conditioning. 2/2 evaluable subjects engrafted at +45 and +90 days. 3 evaluable subjects for toxicity.

Reduced Intensity Conditioning

Patients receiving umbilical cord blood for hematopoietic rescue following non-myeloablative conditioning 1/2 evaluable subjects engrafted at +45 and +90 days. 3 evaluable subjects for toxicity.

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

Analysis denominator · Participants

GroupSource count
Myeloablative Conditioning3
Reduced Intensity Conditioning3

Reported measurements

Source class 1
Values in events · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Myeloablative Conditioning5Not reportedNot reportedNot reportedNot reported
Reduced Intensity Conditioning3Not reportedNot reportedNot reportedNot reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        value
        5
      2. group Id
        OG001
        value
        3
denoms
  1. counts
    1. group Id
      OG000
      value
      3
    2. group Id
      OG001
      value
      3
    units
    Participants
description
Composite endpoint of GVH or infection. Too few events to compare between arms.
groups
  1. description
    Patients receiving umbilical cord blood for hematopoietic rescue following myeloablative conditioning. 2/2 evaluable subjects engrafted at +45 and +90 days. 3 evaluable subjects for toxicity.
    id
    OG000
    title
    Myeloablative Conditioning
  2. description
    Patients receiving umbilical cord blood for hematopoietic rescue following non-myeloablative conditioning 1/2 evaluable subjects engrafted at +45 and +90 days. 3 evaluable subjects for toxicity.
    id
    OG001
    title
    Reduced Intensity Conditioning
param Type
NUMBER
reporting Status
POSTED
time Frame
+180 days
title
Compare Rates of Complications Between Patients Receiving Ablative vs. Non-myeloablative Conditioning Prior to UCB Transplantation
type
SECONDARY
unit Of Measure
events

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

Preserved source evidence · Not medical advice