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NCT01535040 · OUTCOME

Retention

Memantine Hydrochloride in Helping Cancer Survivors Stop Smoking · Source last updated 2021-09-28

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
12 weeks

What was measured

Retention is defined as the percentage of participants who complete the 12 week visit

Analysis population: All randomized participants

Groups in this outcome

Arm I - Memantine

Participants receive memantine hydrochloride PO BID) on days 1-81 in the absence of unacceptable toxicity. memantine hydrochloride: Estimate participation, accrual, adherence, and retention of cancer survivors who smoke and are randomized to receive memantine (10 mg twice daily) or a matching placebo for 12 weeks.

Arm II - Placebo

Participants receive a placebo PO BID on days 1-81 in the absence of unacceptable toxicity. placebo: Placebo by mouth through completion of 12 weeks.

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 I - Memantine65
Arm II - Placebo65

Reported measurements

Source class 1
Values in percentage of participants · Interval/dispersion: 95% Confidence Interval
GroupValueSpreadLowerUpperComment
Arm I - Memantine53.8Not reported41.066.3Not reported
Arm II - Placebo67.7Not reported54.978.8Not reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        lower Limit
        41.0
        upper Limit
        66.3
        value
        53.8
      2. group Id
        OG001
        lower Limit
        54.9
        upper Limit
        78.8
        value
        67.7
denoms
  1. counts
    1. group Id
      OG000
      value
      65
    2. group Id
      OG001
      value
      65
    units
    Participants
description
Retention is defined as the percentage of participants who complete the 12 week visit
dispersion Type
95% Confidence Interval
groups
  1. description
    Participants receive memantine hydrochloride PO BID) on days 1-81 in the absence of unacceptable toxicity. memantine hydrochloride: Estimate participation, accrual, adherence, and retention of cancer survivors who smoke and are randomized to receive memantine (10 mg twice daily) or a matching placebo for 12 weeks.
    id
    OG000
    title
    Arm I - Memantine
  2. description
    Participants receive a placebo PO BID on days 1-81 in the absence of unacceptable toxicity. placebo: Placebo by mouth through completion of 12 weeks.
    id
    OG001
    title
    Arm II - Placebo
param Type
NUMBER
population Description
All randomized participants
reporting Status
POSTED
time Frame
12 weeks
title
Retention
type
PRIMARY
unit Of Measure
percentage of participants

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

Preserved source evidence · Not medical advice