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CompletedNCT02649231KAREUpdated Oct 5, 2021Results posted

Ketamine for Reduction of Alcoholic Relapse

A Phase 2 interventional study of Ketamine and Placebo in Primary Alcohol Use Disorder, sponsored by University College, London. Completed at 2 sites in United Kingdom. Open to participants aged 18 Years to 60 Years. Per ClinicalTrials.gov, last updated 2021-10-05.

Sponsored by University College, London · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
96
Allocation
Randomized
Ages
18 Years to 60 Years
Sex
All
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Study summary

96 recently detoxified alcoholics will be randomized to receive either 3 sessions ketamine (0.8 mg/kg IV over 45 minutes) or placebo plus manualised psychological therapy, or 3 sessions of ketamine or placebo plus simple psychoeducation. Patients will be assessed at 3 and 6 months on a range of psychological and biological variables. Primary endpoints will be % days abstinent at 6 months and relapse rates at 6 months. Secondary endpoints include depressive symptoms, craving, quality of life.

02

Conditions studied

  • Primary Alcohol Use Disorder

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03

In context

Alcoholism

1,606 studies on the registry are indexed under Alcoholism; 329 are open to participants now.

This study's enrollment of 96 is above the median of 87 across 1,371 interventional studies indexed under Alcoholism.

Browse Alcoholism studies →

Lead sponsor

University College, London is the lead sponsor of 632 studies on the registry; 145 are open to participants now.

Of its 6 completed or terminated interventional studies of FDA-regulated products, 2 (33%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Meet either a) DSM-5 criteria for severe alcohol use disorder and b) DSM-IV criteria for alcohol dependence within the last 12 months;
  • Currently abstinent from alcohol (breathalyser BAC level 0.00) and negative urine drug screening (participants testing positive for THC who do not have a history or current cannabis dependency may be included);
  • Minimum of mild depression(>14 on Beck Depression Inventory-II);
  • Capacity to give informed consent as defined by GCP guidelines;
  • Willing and able to wear SCRAM-X bracelet for 6 months;
  • Females of childbearing potential and males must be willing to use an effective method of contraception (hormonal or barrier method of birth control; True abstinence) from the time consent is signed until 6 weeks after treatment discontinuation and inform the trial if pregnancy occurs. For the purpose of clarity, True abstinence is when this is in line with the preferred and usual lifestyle of the subject. Periodic abstinence (e.g., calendar, ovulation, symptothermal, post-ovulation methods), declaration of abstinence, withdrawal, spermicides only or lactational amenorrhoea method for the duration of a trial, are not acceptable methods of contraception;
  • Females of childbearing potential must have a negative pregnancy test within 7 days prior to being registered for trial treatment and on day of first treatment.

Exclusion criteria

Exclusion Criteria:

  • Currently taking any other relapse prevention medication or anti-depressants;
  • Uncontrolled hypertension, systolic 140mm Hg or greater and diastolic 90mm Hg or greater;
  • \<16 or > 35 BMI
  • History of psychosis, or in a first-degree relative as identified by DSM-5 or DSM-IV SCID; co-morbid current psychiatric diagnosis excluding depression, identified via self-reported or identified by a medical professional;
  • Previous or current diagnosis of substance dependence / severe substance misuse disorder;
  • History of neuropsychological difficulties
  • One or more previous confirmed seizures;
  • Currently taking daily prescribed medication contraindicated in the SPC with ketamine:

    1. Barbiturates and/or narcotics
    2. Atracurium and tubocurarine
    3. Central nervous system (CNS) depressants (e.g. phenothiazines, sedating H1 - blockers or skeletal muscle relaxants)
    4. Anxiolytics, sedatives and hypnotics
    5. Thiopental, thyroid hormones
    6. Antihypertensive agents
    7. Theophylline and methylxanthines.
    8. Halogenated anaesthetics
    9. OR psychotropic drug use at screening assessments or during treatment weeks
  • Liver function tests > 3 times normal levels
  • Where there are "special warnings or precautions for use" according to the SPC and where risk vs benefit ratio is not in favour of giving ketamine, with assessment made by physical examination by medically qualified trial personnel, self-report or inspection of the medical notes:

    1. Acute intermittent porphyria
    2. Dehydration or hypovolemia
    3. Hyperthyroidism, or patients receiving thyroid replacement
    4. Pulmonary or upper respiratory tract infection
    5. Severe Coronary artery disease, Cerebrovascular accident or cerebral trauma
    6. Diabetes
    7. Known glaucoma or globe injuries
    8. Cirrhosis
    9. Epilepsy
    10. Neurological condition/brain damage
    11. Intracranial mass lesions, presence of head injury or hydrocephalus
  • Suicidal ideation.
  • Not willing to use effective contraception or (females) take pregnancy test;
  • Allergic reaction to ketamine;
  • >10 previous detoxifications from alcohol;
  • Pregnant or breastfeeding;
  • Allergies to excipients of IMP or placebo;
  • Use of another experimental investigational medicinal product that is likely to interfere with the study medication within 3 months of study enrolment.
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
96 participants (actual)

Study arms

  • Experimental
    Ketamine+Psychological Therapy

    Ketamine with psychological therapy

    Drug: Ketamine · Behavioral: Psychological Therapy

  • Active comparator
    Ketamine+Education

    ketamine with alcohol education

    Drug: Ketamine · Behavioral: Alcohol Education

  • Active comparator
    Placebo+Psychological Therapy

    placebo with psychological therapy

    Drug: Placebo · Behavioral: Psychological Therapy

  • Placebo comparator
    Placebo+Education

    placebo with simple alcohol education

    Drug: Placebo · Behavioral: Alcohol Education

Interventions

  • DrugKetamine

    0.8 mg/kg ketamine

  • DrugPlacebo

    0.9% saline

  • BehavioralPsychological Therapy

    Manualised relapse prevention based CBT

  • BehavioralAlcohol Education

    Simple education about alcohol effects

06

What researchers measure

Primary outcomes

  1. Relapse Rates

    Time line follow back

    Time frame: 6 months

  2. Percentage Days Abstinent

    Time line follow back

    Time frame: 6 months

07

Results

Posted Sep 9, 2021

Participant flow

Participant flow — Overall Study
MilestoneKetamine+Psychological TherapyKetamine+EducationPlacebo+Psychological TherapyPlacebo+Education
Started24242325
Completed20212123
Not completed4322
Withdrew: Adverse event0001
Withdrew: Lost to follow-up2110
Withdrew: Withdrawal by subject0101
Withdrew: Protocol violation2110

Outcome measures

PrimaryRelapse Rates

Time line follow back

Time frame:
6 months
Reported as:
Count of participants · Participants
Relapse Rates
ParticipantsKetamine+Psychological TherapyKetamine+EducationPlacebo+Psychological TherapyPlacebo+Education
Relapse Rates13151418
Statistical analysis
  • Ketamine+Psychological Therapy vs Ketamine+Education vs Placebo+Psychological Therapy vs Placebo+Education · Odds ratio (or): 0.7 · 95% CI 0.28 to 1.75
PrimaryPercentage Days Abstinent

Time line follow back

Time frame:
6 months
Reported as:
Mean · percentage of days abstinent
Percentage Days Abstinent
percentage of days abstinentKetamine+Psychological TherapyKetamine+EducationPlacebo+Psychological TherapyPlacebo+Education
Percentage Days Abstinent86.4 ± 17.782.5 ± 20.078.3 ± 26.970.7 ± 25.1
Statistical analysis
  • Ketamine+Psychological Therapy vs Ketamine+Education vs Placebo+Psychological Therapy vs Placebo+Education · Mean difference (final values): 10.1 · 95% CI 1.1 to 19.0

Adverse events

Collected over Screening visit (visit 1) to 6 month follow-up visit (visit 10).Participants were asked about any potential adverse events at the beginning of each visit.. Non-serious events are listed at a 4% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Ketamine+Psychological Therapy0/24 (0%)0/24 (0%)13/24 (54.2%)
Ketamine+Education0/24 (0%)0/24 (0%)17/24 (70.8%)
Placebo+Psychological Therapy0/23 (0%)2/23 (8.7%)16/23 (69.6%)
Placebo+Education0/25 (0%)1/25 (4%)17/25 (68%)
Most frequent serious events
Most frequent serious events
EventKetamine+Psychological TherapyKetamine+EducationPlacebo+Psychological TherapyPlacebo+Education
Abdominal painPregnancy, puerperium and perinatal conditions0/240/241/230/25
Kidney infectionInfections and infestations0/240/241/230/25
Brain hemorrhageInjury, poisoning and procedural complications0/240/240/231/25
Alcohol intoxicationGeneral disorders0/240/240/231/25
Skull fractureInjury, poisoning and procedural complications0/240/240/231/25
Most frequent other events
Showing 10 of 111
Most frequent other events
EventKetamine+Psychological TherapyKetamine+EducationPlacebo+Psychological TherapyPlacebo+Education
Depressed moodPsychiatric disorders4/2412/247/236/25
HeadacheNervous system disorders3/244/242/238/25
FatigueGeneral disorders3/246/240/234/25
Impaired concentrationNervous system disorders0/244/241/232/25
HaematomaInjury, poisoning and procedural complications0/241/240/234/25
Viral rhinitisRespiratory, thoracic and mediastinal disorders1/242/242/234/25
AnxietyPsychiatric disorders2/241/243/233/25
Memory impairmentNervous system disorders1/243/240/232/25
InsomniaGeneral disorders2/242/242/232/25
DizzinessNervous system disorders2/241/242/230/25

Baseline characteristics

Age, Continuous
Age, Continuous(years)Ketamine+Psychological TherapyKetamine+EducationPlacebo+Psychological TherapyPlacebo+EducationTotal
Mean45.2 ± 8.740.5 ± 11.147.0 ± 11.843.7 ± 10.244.1 ± 10.6
Sex: Female, Male
Sex: Female, Male(Participants)Ketamine+Psychological TherapyKetamine+EducationPlacebo+Psychological TherapyPlacebo+EducationTotal
Female10781035
Male1417151561
Race and Ethnicity Not Collected
Race and Ethnicity Not Collected(Participants)Ketamine+Psychological TherapyKetamine+EducationPlacebo+Psychological TherapyPlacebo+EducationTotal
Count of participants————0
Region of Enrollment
Region of Enrollment(participants)Ketamine+Psychological TherapyKetamine+EducationPlacebo+Psychological TherapyPlacebo+EducationTotal
United Kingdom2424232596
08

Study locations

2 sites
  • NIHR Exeter Clinical Research Facility
    Exeter, EX4 5DW, United Kingdom
  • NIHR UCLH Clinical Research Facility
    London, NW1 2BU, United Kingdom
09

References and documents

Publications

  • Grabski M, McAndrew A, Lawn W, Marsh B, Raymen L, Stevens T, Hardy L, Warren F, Bloomfield M, Borissova A, Maschauer E, Broomby R, Price R, Coathup R, Gilhooly D, Palmer E, Gordon-Williams R, Hill R, Harris J, Mollaahmetoglu OM, Curran HV, Brandner B, Lingford-Hughes A, Morgan CJA. Adjunctive Ketamine With Relapse Prevention-Based Psychological Therapy in the Treatment of Alcohol Use Disorder. Am J Psychiatry. 2022 Feb;179(2):152-162. doi: 10.1176/appi.ajp.2021.21030277. Epub 2022 Jan 11. PubMed 35012326 ↗
  • Grabski M, Borissova A, Marsh B, Morgan CJA, Curran HV. Ketamine as a mental health treatment: Are acute psychoactive effects associated with outcomes? A systematic review. Behav Brain Res. 2020 Aug 17;392:112629. doi: 10.1016/j.bbr.2020.112629. Epub 2020 May 30. PubMed 32485203 ↗
  • McAndrew A, Lawn W, Stevens T, Porffy L, Brandner B, Morgan CJ. A proof-of-concept investigation into ketamine as a pharmacological treatment for alcohol dependence: study protocol for a randomised controlled trial. Trials. 2017 Apr 4;18(1):159. doi: 10.1186/s13063-017-1895-6. PubMed 28372596 ↗

Study documents

  • Study protocol · Jan 20, 2020
  • Statistical analysis plan · Mar 11, 2020

Documents are hosted by the registry — open the source record to download them.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 5, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02649231
Lead sponsor
University College, London
Responsible party
Sponsor
First posted
Jan 7, 2016
Start date
Oct 2016
Primary completion
Feb 2020
Completion
Feb 2020
Results posted
Sep 9, 2021
Last update
Oct 5, 2021

Study contacts

Celia Morgan, Ph.D.
principal investigator · UCL

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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