Evidence map›Paper›PMID 40340434›Full record

Trial reportCancer control : journal of the Moffitt Cancer Center

Randomized Placebo-Controlled Trial of Memantine for Smoking Cessation (CCCWFU 99311).

John Spangler, Elizabeth Skidmore, Emily V Dressler, Kathryn E Weaver, Glenn J Lesser, Gary Burton, Benjamin Esparaz, Brooke Gillett, Edward G Shaw

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Cancer control : journal of the Moffitt Cancer Center. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

John SpanglerDepartment of Family and Community Medicine, Wake Forest University School of Medicine, Winston-Salem, NC, USA.ORCID 0000-0002-7949-7050
Elizabeth SkidmoreDepartment of Family and Community Medicine, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
Emily V DresslerDepartment of Biostatistics and Data Science, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
Kathryn E WeaverDepartment of Social Sciences and Health Policy, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
Glenn J LesserDepartment of Internal Medicine, Section on Hematology and Oncology, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
Gary BurtonDivision of Hematology and Oncology, Louisiana State University Feist-Weiller Cancer Center, Shreveport, LA, USA.
Benjamin EsparazCentral Illinois Community Clinical Oncology Program, Cancer Care Specialists of Central Illinois, Decatur, IL, USA.
Brooke GillettCentral Illinois Community Clinical Oncology Program, Cancer Care Specialists of Central Illinois, Decatur, IL, USA.
Edward G ShawDepartment of Internal Medicine, Section of Gerontology and Geriatric Medicine, Wake Forest University School of Medicine, Winston-Salem, NC, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

IntroductionQuitting smoking is challenging even with existing pharmacotherapy. Thus, discovery of new cessation medications is imperative. Memantine, a well-tolerated Alzheimer's disease drug, partially antagonizes glutamate at the N-methyl-D-Aspartate receptor (NMDAR), modulating dopamine release in addiction pathways. Memantine may interrupt nicotine reward and promote smoking cessation.Materials and MethodsAt 23 community oncology practices nationwide, we recruited 130 breast, prostate, lung, or colorectal cancer survivors ≥ six months beyond definitive treatment who currently smoked at least 10 cigarettes daily and wanted to quit. In a double-blind fashion, participants were randomized to take either memantine (10 mg) or a matching placebo twice daily for 12 weeks (65 per arm). Toxicity, nicotine dependence, and past-week abstinence were recorded at 2, 4-, 6-, 9-, and 12-weeks post-randomization. The primary endpoint was feasibility and preliminary estimation of 12-week self-reported past-week smoking abstinence.ResultsThere were no significant differences in abstinence rates or nicotine dependence between the two groups at 12 weeks. Twelve-week completion of therapy was low, but lower in memantine than control participants (42% vs 63%, respectively;

Indexed as

MemantineSmoking CessationAgedDouble-Blind MethodFemaleHumansMaleMiddle AgedTobacco Use DisorderTreatment OutcomeMemantinecancer survivorsmemantinenicotine addictionsmoking cessationtobacco use

Identifiers

PMID40340434
PMCPMC12062594

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.