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NCT02599194 · OUTCOME

Number of Treatment-Related Adverse Events

18F-FSPG PET/CT for Cancer Patients on Therapy · Source last updated 2019-01-03

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

Measure
NUMBER
Unit
adverse events
Interval / dispersion
Not reported
Time frame
Baseline to up to 2 years

What was measured

Safety and tolerability of 18F-FSPG and 18F-FDG were assessed as treatment-related adverse events, and reported as the number of events related to each treatment, without dispersion.

Groups in this outcome

18F-FSPG and 18F-FDG Intragroup Comparision

Participants sequentially receive radioimaging agents 18F-FSPG and 18F-FDG IV followed by PET/CT scan with 60 minutes. 18F-FSPG: Administered intravenously (IV) 18F-FDG: Administered intravenously (IV)

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

Analysis denominator · Participants

GroupSource count
18F-FSPG and 18F-FDG Intragroup Comparision7

Reported measurements

18F-FSPG
Values in adverse events · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
18F-FSPG and 18F-FDG Intragroup Comparision0Not reportedNot reportedNot reportedNot reported
18F-FDG
Values in adverse events · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
18F-FSPG and 18F-FDG Intragroup Comparision0Not reportedNot reportedNot reportedNot reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        value
        0
    title
    18F-FSPG
  2. categories
    1. measurements
      1. group Id
        OG000
        value
        0
    title
    18F-FDG
denoms
  1. counts
    1. group Id
      OG000
      value
      7
    units
    Participants
description
Safety and tolerability of 18F-FSPG and 18F-FDG were assessed as treatment-related adverse events, and reported as the number of events related to each treatment, without dispersion.
groups
  1. description
    Participants sequentially receive radioimaging agents 18F-FSPG and 18F-FDG IV followed by PET/CT scan with 60 minutes. 18F-FSPG: Administered intravenously (IV) 18F-FDG: Administered intravenously (IV)
    id
    OG000
    title
    18F-FSPG and 18F-FDG Intragroup Comparision
param Type
NUMBER
reporting Status
POSTED
time Frame
Baseline to up to 2 years
title
Number of Treatment-Related Adverse Events
type
SECONDARY
unit Of Measure
adverse events

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

Preserved source evidence · Not medical advice