Evidence map›Paper›PMID 40342163›Full record

Trial reportPsychopharmacology2025

A Mechanistic study assessing difficulty discontinuing chronic hypnotic use.

Timothy Roehrs, Gail Koshorek, Mohammad Sibai, Aisha Tabor, Luisa Bazan, Thomas Roth

Abstract readRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Psychopharmacology, 2025. 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

6 authors.

Timothy RoehrsHenry Ford Health System, Sleep Disorders and Research Center & Research Ctr Henry Ford Hospital, 2799 West Grand Blvd, CPF-3 Detroit, MI, 48202, USA. troehrs1@hfhs.org.ORCID http://orcid.org/0000-0001-9237-0153
Gail KoshorekHenry Ford Health System, Sleep Disorders and Research Center & Research Ctr Henry Ford Hospital, 2799 West Grand Blvd, CPF-3 Detroit, MI, 48202, USA.
Mohammad SibaiHenry Ford Health System, Sleep Disorders and Research Center & Research Ctr Henry Ford Hospital, 2799 West Grand Blvd, CPF-3 Detroit, MI, 48202, USA.
Aisha TaborHenry Ford Health System, Sleep Disorders and Research Center & Research Ctr Henry Ford Hospital, 2799 West Grand Blvd, CPF-3 Detroit, MI, 48202, USA.
Luisa BazanHenry Ford Health System, Sleep Disorders and Research Center & Research Ctr Henry Ford Hospital, 2799 West Grand Blvd, CPF-3 Detroit, MI, 48202, USA.
Thomas RothHenry Ford Health System, Sleep Disorders and Research Center & Research Ctr Henry Ford Hospital, 2799 West Grand Blvd, CPF-3 Detroit, MI, 48202, USA.

Funding

National Institute of Drug Abuse DA R01038177
6 · The paper itself

Abstract

rationaleThe abuse liability of chronic hypnotic use remains a clinical concern.

objectivesThis study assessed 1) whether there would be greater difficulty discontinuing chronic hypnotic use for people with insomnia and hyperarousal vs those with insomnia but without hyperarousal and 2) whether those seeking to discontinue chronic hypnotic use of the receptor non-specific hypnotic eszopiclone would have more difficulty than those discontinuing the receptor specific zolpidem XR.

methodsDSM-V diagnosed insomnia participants, aged 23-61 yrs, (n = 41, 36 females), with no other sleep disorders, unstable medical or psychiatric diseases or drug dependency completed the trial. Following a screening nocturnal polysomnogram (NPSG) participants were randomized to zolpidem XR (12.5 mg), eszopiclone (3 mg), or placebo nightly for 6 months. After 6 months nightly use, over a 2-week discontinuation, they were instructed to discontinue their hypnotic use, but, if necessary, to self-administer before sleep either 1, 2, or 3 capsules, each packaged separately in envelopes labeled 1, 2, and 3, containing their assigned "blinded" medication or placebo.

resultsOver the 14 nights 21 participants took zero (51%) capsules and among the 20 taking capsules the median total number chosen was 3. Those people with insomnia and hyperarousal vs those with insomnia but not hyperarousal had more difficulty discontinuing chronic hypnotic use (aim 1) as did those using eszopiclone vs zolpidem or placebo (aim 2).

conclusionsMost subjects discontinued hypnotic use and among the few continuing to use their use declined from week one to week two of the discontinuation period.

Indexed as

Azabicyclo CompoundsHypnotics and SedativesPiperazinesPyridinesSleep Initiation and Maintenance DisordersAdultArousalDouble-Blind MethodEszopicloneFemaleHumansMaleMiddle AgedPolysomnographyYoung AdultZolpidemAzabicyclo CompoundsEszopicloneHypnotics and SedativesPiperazinesPyridinesZolpidemChronic insomniaDiscontinuing hypnotic useEszopicloneZolpidem XR

Identifiers

What OpenQuestion holds

Textmetadata
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Registered trials

None linked

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.