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Completed

NCT Number: NCT05902819

Reconsolidation Blockade of Intrusive Trauma- and Cocaine-related Memories

An investigation of the effect of matrix-metalloproteinase-(MMP)-9 inhibition with minocycline on the reconsolidation of trauma- or cocaine-related memories

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Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University Hospital of Psychiatry Zurich, University of Zurich

Zurich, 8032, Switzerland

About this study

Intrusive memories are involuntary recollections of past emotional events that can become pathological and persist over time, particularly in post-traumatic stress disorder (PTSD) and cocaine use disorders (CUD). Both PTSD and CUD are characterised by a hypersensitivity and -reactivity to cue-elicited memory reactivation and exhibit common neurological alterations, suggesting shared underlying mechanisms. As intrusive memories significantly contribute to maintaining the cycle of relapse in both disorders, it is important to find a way to attenuate them successfully. Research on memory reconsolidation has led to the development of different (pharmacological) approaches to disrupt the process, which have, however, yielded mixed and unspecific effects so far.

The present project aims to investigate the effect of MMP-9 inhibition with minocycline on the reconsolidation of intrusive memories in individuals with CUD or PTSD. Participants will be randomly assigned to a minocycline or placebo group. The study comprises a total of 5 visits during 3 weeks and one follow-up online survey (3 months after the intervention). Participants will receive the study medication before two imagery script-guided memory activation sessions. An ecological momentary assessment (EMA) approach will be employed to track intrusive memories, and glutamate concentration and neural activation will be measured with magnetic resonance spectroscopy (MRS) and functional magnetic resonance (fMRI), respectively, before and after the two imagery sessions.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

General Inclusion Criteria:

  • Ability to read, understand and provide written informed consent
  • Age between 18 and 60 years
  • To be sufficiently fluent in German

Inclusion criteria

for the PTSD group:

  • Current diagnosis of full PTSD according to the 5th version of the Diagnostic and Statistical Manual of Mental Disorders (DSM-5), of subthreshold PTSD, as in meeting two to three of the DSM-5 criteria B-E, or of complex PTSD

Inclusion criteria

for the CUD group:

  • Current diagnosis of mild, moderate, or severe CUD according to DSM-5
  • Regular cocaine use in the last 12 months and at least one consumption event in the last 6 months

Inclusion criteria

for the Clinical Controls (PTSD+CUD group):

  • Current diagnosis of full PTSD according to the 5th version of the Diagnostic and Statistical Manual of Mental Disorders (DSM-5), of subthreshold PTSD, as in meeting two to three of the DSM-5 criteria B-E, or of complex PTSD
  • Current diagnosis of mild, moderate, or severe CUD according to DSM-5
  • Regular cocaine use in the last 12 months and at least one consumption event in the last 6 months

Exclusion criteria

for the HC, PTSD, CUD, and PTSD+CUD groups:

  • Women who are pregnant or breast feeding or intending to become pregnant during the course of the study or within 3 months after
  • Other clinically significant concomitant disease states, e.g., renal failure (i.e., estimated glomerular filtration rate (eGFR; CKD-EPI) lower than 60 ml/min/1.73 m2), hepatic dysfunction (i.e., alanine transaminase (ALT) higher than 90 U/I for women or 110 U/I for men, aspartate aminotransferase (AST) higher than 74 U/I, and/or gamma-glutamyl transferase (γGT) higher than 70 U/I for women or 120 U/I for men), cardiovascular disease, etc.
  • Presence or history of severe neurological disorders, head injuries or systemic/rheumatic disease
  • Diagnosis of schizophrenia, bipolar disorder, or autism spectrum disorder according to DSM-5
  • Pacemaker, neurostimulator or any other head or heart implants as well as MRI-incompatible metal parts or possibility of metal fragments in the body (MR safety)
  • Claustrophobia (MR safety)
  • Dependence on a hearing aid (MR safety)
  • Inability to follow the procedures of the study, e.g., due to language problems
  • Participation in another study with investigational drugs within the 30 days preceding and during the present study
  • More than three suicide attempts in the past, a suicide attempt within the last 12 months and/or acute suicidality

Exclusion criteria

for Healthy Controls:

  • Any current psychiatric diagnosis according to DSM-5 except for mild or moderate substance use disorder (SUD) for nicotine, and mild SUD for alcohol and cannabis
  • Diagnosis of CUD according to DSM-5 (lifetime)
  • Diagnosis of PTSD according to DSM-5 (lifetime)

Exclusion criteria

for both the PTSD and CUD groups:

  • Allergy to minocycline or to any other ingredient in the named drug
  • Current intake of the following medications interacting with minocycline: acitretin, acetylcystein, aluminiumhydroxid, amitryptiline, any antibiotics, antidiabetic drug such as sulfonylurea, atazanavir, atomoxetine, anticoagulant drugs from the coumarin type, barbiturates, bupropion, carbamazepine, ciclosporin A, isotretinoin, methotrexate, phenytoin, and theophylline

Exclusion criteria

for only the PTSD group:

  • Diagnosis of CUD according to DSM-5 (lifetime)
  • Current diagnosis of severe SUD for nicotine, moderate SUD for alcohol and cannabis, and mild SUD for all other substances according to DSM-5

Exclusion criteria

for only the CUD group:

  • Diagnosis of PTSD according to DSM-5 (lifetime)
  • Current diagnosis of severe SUD for alcohol or cannabis, and mild SUD for all other substances (except for nicotine) according to DSM-5

Exclusion criteria

for Clinical Controls (PTSD+CUD group):

  • Current diagnosis of severe SUD for alcohol or cannabis, and mild SUD for all other substances (except for nicotine) according to DSM-5

Treatment and study plan

Imagery

Behavioral

Guided imagery of personal trauma- or cocaine-related memory approximately 120min after study medication was given.

Minocycline

Drug

Single dose of minocycline (200mg) at each of two imagery sessions; Minocycline is given orally in form of a capsule.

Placebo

Drug

Single dose of mannitol (100%) at each of two imagery sessions; Placebo is given orally in form of a capsule.

Primary outcomes

  1. Changes in intrusive memories frequency and features

    Time frame: Changes from baseline intrusive memories frequency and features after both 9 to 39 days (follow-up 1) and approx. 3.5 months (follow-up 2)

    Measured with the Intrusion Questionnaire, containing various items on intrusive memories frequency, arousal and distress as well as triggers, and responses.

  2. Change over time in self-reported intrusive memories frequency, arousal and distress

    Time frame: EMA will be conducted for an average of 12 to 42 days (through study participation from baseline to 3 days after follow-up 1).

    Captured with a short version of the Intrusion Questionnaire implemented as smartphone-based ecological momentary assessment (EMA), containing items on arousal and distress from self-reported intrusive memories.

Secondary outcomes

  1. Changes in MRS signal parameters

    Time frame: Change from baseline MRS-measured glutamate concentrations after 9 to max. 39 days (follow-up 1).

    Glutamate concentrations are measured using MRS in the amygdala in the PTSD group and in the nucleus accumbens in the CUD group.

  2. Changes in fMRI Blood-Oxygenation-Level Dependent (BOLD) contrasts

    Time frame: Changes from baseline fMRI BOLD contrasts after 9 to max. 39 days (follow-up 1).

    fMRI BOLD contrasts between conditions (neutral/stress/trauma for the PTSD group; neutral/reward/drug for the CUD group) and between groups.

  3. Change in heart rate variability (HRV) during fMRI memory reactivation

    Time frame: Change from baseline HRV after 9 to max. 39 days (follow-up 1).

    HRV will be measured during the fMRI cue-reactivity paradigm (listening to trauma- or cocaine-related narratives compared to trauma- and cocaine-unrelated narratives).

  4. Change in respiratory rate during fMRI memory reactivation

    Time frame: Change from baseline respiratory rate after 9 to max. 39 days (follow-up 1).

    Respiratory rate will be measured during the fMRI cue-reactivity paradigm (listening to trauma- or cocaine-related narratives compared to trauma- and cocaine-unrelated narratives).

  5. Change in subjective rating of distress before and after memory reactivation

    Time frame: Change from baseline subjective distress after 9 to max. 39 days (follow-up 1).

    Current subjective distress will be measured with a visual analogue scale before and after listening to trauma- and cocaine-related narratives compared to trauma- and cocaine-unrelated narratives.

  6. Change in subjective rating of craving before and after memory reactivation

    Time frame: Change from baseline craving after 9 to max. 39 days (follow-up 1).

    Current subjective craving will be measured with the Cocaine Craving Questionnaire (containing ten questions on current craving scaled from 0 to 10) before and after listening to cocaine-related narratives compared to cocaine-unrelated narratives.

  7. Change in neurofilament light chain (NfL) levels

    Time frame: Change from baseline NfL levels after 9 to max. 39 days (follow-up 1).

    NfL levels will be measured in serum samples.

  8. Change in sphingolipid levels

    Time frame: Change from baseline sphingolipid levels after 9 to max. 39 days (follow-up 1).

    Sphingolipid levels will be measured in plasma samples.

  9. Change in inflammatory biomarker levels

    Time frame: Change from baseline inflammatory levels after 9 to max. 39 days (follow-up 1).

    Inflammatory biomarker levels will be measured in serum samples.

  10. Change in MMP-9 protein levels

    Time frame: Change from baseline MMP-9 protein levels after 9 to max. 39 days (follow-up 1).

    MMP-9 protein levels will be measured in plasma samples.

  11. Change in MMP-9 gene expression

    Time frame: Change from baseline MMP-9 gene expression after 9 to max. 39 days (follow-up 1).

    MMP-9 gene expression will be measured in blood samples.

  12. Heartrate variability

    Time frame: Will be measured during 9 to max. 39 days, from baseline until follow-up 1.

    Heartrate variability (measured with a wearable (Fitbit)) predicted by the number and quality of intrusive memories experienced. Overall variability per person, in relation to overall health measured at Screening and Baseline as well as pre- and post-intervention variability will be assessed.

  13. Sleep duration

    Time frame: Will be measured during 9 to max. 39 days, from baseline until follow-up 1.

    Sleep duration (in minutes), trajectories over the course of the study periods, clusters of variations in duration and sleep quality (as averaged by the algorithm of Fitbit), according to medication/placebo, number of intrusions and overall health measured at Screening and Baseline.

  14. Change in Obsessive Compulsive Cocaine Use Scale (OCCUS)

    Time frame: Change from baseline OCCUS score after both 9 to 39 days (follow-up 1) and approx. 3.5 months (follow-up 2).

    A 14-item self-report measure that assesses the current inability to control or resist cocaine-related thoughts and behaviors, frequency and impact of thoughts and impulses related to cocaine use, and the degree of interference caused by cocaine related thoughts and behaviors.

  15. PTSD Checklist for DSM-5 (PCL-5)

    Time frame: Change from baseline PCL-5 score after both 9 to 39 days (follow-up 1) and approx. 3.5 months (follow-up 2).

    A 20-item self-report measure that assesses the 20 DSM-5 symptoms of PTSD in the last 2 weeks prior to the visit.

  16. Beck Depression Inventory-II (BDI-II)

    Time frame: Change from baseline BDI-II score after both 9 to 39 days (follow-up 1) and approx. 3.5 months (follow-up 2).

    A 21-item self-report measure for assessing the severity of depression in the last 2 weeks prior to the visit.

  17. Pittsburgh Sleep Quality Index (PSQI)

    Time frame: Change from baseline PSQI score after both 9 to 39 days (follow-up 1) and approx. 3.5 months (follow-up 2).

    A 19-item self-report measure which assesses sleep quality and disturbances in the last 2 weeks prior to the visit.

  18. Global Assessment of Functioning (GAF)

    Time frame: Change from screening GAF score after both 10 to 50 days (follow-up 1) and approx. 4 months (follow-up 2).

    A numeric scale used by the investigators to rate the current social, occupational, and psychological functioning of a participants. Scores range from 100 (extremely high functioning) to 1 (severely impaired).

  19. Clinician-Administered PTSD Scale for DSM-5 (CAPS-5)

    Time frame: Change from screening CAPS-5 score after approx. 4 months (follow-up 2).

    A 30-item structured interview that is used to assess the 20 DSM-5 PTSD symptoms, subjective distress, impact of symptoms on social and occupational functioning, improvement in symptoms since the previous CAPS administration, and overall PTSD severity, and specifications for the dissociative subtype.

  20. Changes in the Interview for Psychotropic Drug Consumption (IPDC)

    Time frame: Change from screening IPDC after approx. 4 months (follow-up 2).

    A structured interview assessing self-reported patterns of use of common licit and illicit substances during the most representative month of the past year and, in the case of regular cocaine use, also specifically during the past month.

  21. Voice-recorded language features of memories

    Time frame: Assessed at screening

    Voice features and text-based features of reported autobiographical memories recorded during the screening to predict symptoms, with a primary focus on the prediction of intrusion-related features.

Sponsors and collaborators

Lead sponsor

Psychiatric University Hospital, Zurich

Other

Collaborators

  • University of Zurich

Registry information

Official study title

An Investigation of the Effect of MMP-9 Inhibition With Minocycline on the Reconsolidation of Intrusive Trauma- or Cocaine-related Memories

Acronym: Memocycline

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Jun 15, 2023
Registry last updated
Mar 6, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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