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NCT00534001 · OUTCOME

Abstinence

Bupropion in Helping Adults Stop Smoking · Source last updated 2017-05-30

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

Measure
COUNT_OF_PARTICIPANTS
Unit
Participants
Interval / dispersion
Not reported
Time frame
4 weeks

What was measured

Bioverified 4-week continuous abstinence

Groups in this outcome

Arm I (1-week run-in)

Participants receive an oral placebo once or twice daily in weeks 1-3 followed by oral bupropion hydrochloride once or twice daily in week 4. Participants also undergo 90-minute behavioral group counseling sessions once in weeks 1, 2, and 4. bupropion hydrochloride: Given orally placebo: Given orally

Arm II (4-week run-in)

Participants receive oral bupropion hydrochloride once or twice daily in weeks 1-4. Participants also undergo 90-minute behavioral group counseling sessions once in weeks 1, 2, and 4. bupropion hydrochloride: Given orally

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 (1-week run-in)48
Arm II (4-week run-in)47

Reported measurements

Source class 1
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm I (1-week run-in)25Not reportedNot reportedNot reportedNot reported
Arm II (4-week run-in)15Not reportedNot reportedNot reportedNot reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        value
        25
      2. group Id
        OG001
        value
        15
denoms
  1. counts
    1. group Id
      OG000
      value
      48
    2. group Id
      OG001
      value
      47
    units
    Participants
description
Bioverified 4-week continuous abstinence
groups
  1. description
    Participants receive an oral placebo once or twice daily in weeks 1-3 followed by oral bupropion hydrochloride once or twice daily in week 4. Participants also undergo 90-minute behavioral group counseling sessions once in weeks 1, 2, and 4. bupropion hydrochloride: Given orally placebo: Given orally
    id
    OG000
    title
    Arm I (1-week run-in)
  2. description
    Participants receive oral bupropion hydrochloride once or twice daily in weeks 1-4. Participants also undergo 90-minute behavioral group counseling sessions once in weeks 1, 2, and 4. bupropion hydrochloride: Given orally
    id
    OG001
    title
    Arm II (4-week run-in)
param Type
COUNT_OF_PARTICIPANTS
reporting Status
POSTED
time Frame
4 weeks
title
Abstinence
type
SECONDARY
unit Of Measure
Participants

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

Preserved source evidence · Not medical advice