NCT07434401

Brief Summary

This cross-sectional observational cohort study examined serum α-N-acetylgalactosaminidase levels in methamphetamine use disorder (MUD), methamphetamine-induced psychotic disorder (MP), and healthy control (HC) groups. The study aimed to determine whether decreased α-N-acetylgalactosaminidase levels are associated with psychotic symptoms in methamphetamine users.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
93

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started May 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 1, 2025

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 31, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 31, 2025

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

February 20, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

February 25, 2026

Completed
Last Updated

February 25, 2026

Status Verified

February 1, 2026

Enrollment Period

4 months

First QC Date

February 20, 2026

Last Update Submit

February 20, 2026

Conditions

Keywords

α-N-acetylgalactosaminidaseMethamphetaminePsychotic DisorderMethamphetamine PsychosisPsychostimulants

Outcome Measures

Primary Outcomes (1)

  • α-N-acetylgalactosaminidase

    Serum α-N-acetylgalactosaminidase levels measured by ELISA (ng/mL).

    At hospital admission (baseline)

Secondary Outcomes (2)

  • Aggregate Index of Systemic Inflammation (AISI)

    At hospital admission (baseline)

  • Positive and Negative Syndrome Scale (PANSS) Score

    At hospital admission (baseline)

Study Arms (3)

Methamphetamine Use Disorder

Adult participants (18-65 years) diagnosed with Methamphetamine Use Disorder according to DSM-5-TR criteria. Participants were evaluated at hospital admission (baseline). No intervention was assigned by the study protocol. Blood samples were collected for measurement of serum α-N-acetylgalactosaminidase levels and complete blood count parameters. No psychometric scales were administered to this group. Sociodemographic and clinical data were recorded for all participants.

Methamphetamine-Induced Psychotic Disorder

Adult participants (18-65 years) diagnosed with Methamphetamine-Induced Psychotic Disorder according to DSM-5-TR criteria. Participants were evaluated at hospital admission (baseline). No intervention was assigned by the study protocol. Blood samples were collected for measurement of serum α-N-acetylgalactosaminidase levels and complete blood count parameters. Psychotic symptom severity was assessed using the Positive and Negative Syndrome Scale (PANSS). Sociodemographic and clinical data were recorded for all participants.

Healthy Control

Healthy control adult participants (18-65 years) without any current or past psychiatric disorder. No intervention was administered as part of the research protocol. Participants underwent a baseline clinical evaluation and provided a single blood sample for measurement of serum α-N-acetylgalactosaminidase levels and complete blood count inflammatory markers. Sociodemographic and clinical data were recorded for all participants.

Eligibility Criteria

Age18 Years - 65 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The study population consisted of adult male inpatients aged 18-49 years who were admitted to Elazığ Mental Health and Diseases Hospital between May 1, 2025 and August 31, 2025. The MP group included consecutive inpatients diagnosed with methamphetamine-induced psychotic disorder and the MUD group included consecutive inpatients diagnosed with methamphetamine use disorder according to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision (DSM-5-TR). Both patient groups consisted of active methamphetamine users and were hospitalized for clinical management at the time of assessment. Urine toxicology screening was performed at admission to confirm substance use status. The Healthy Control (HC) group consisted of adult male individuals without current or past psychiatric disorders and without substance use disorders, matched to patient groups in terms of age and body mass index. HCs had no significant medical illnesses.

You may qualify if:

  • Diagnosis of MUD according to DSM-5-TR
  • Medication-free for at least one month prior to admission
  • Age ≥ 18 years and \<65 years
  • Provided informed consent
  • For Methamphetamine Use Disorder (MUD) Group:

You may not qualify if:

  • Hypertension
  • Diabetes mellitus
  • Chronic kidney disease
  • Rheumatoid arthritis
  • Systemic lupus erythematosus
  • Cardiac illness
  • Severe neurological disorders
  • Immunological or systemic illness
  • Primary psychiatric disorders other than MUD
  • Alcohol use disorder
  • For Methamphetamine-Induced Psychotic Disorder (MP) Group:
  • Diagnosis of MP according to DSM-5-TR
  • Medication-free for at least one month prior to admission
  • Age ≥ 18 years and \<65 years
  • Provided informed consent
  • +28 more criteria

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Elazığ Mental Health and Diseases Hospital

Elâzığ, Elâzığ, 23200, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Psychotic Disorders

Condition Hierarchy (Ancestors)

Schizophrenia Spectrum and Other Psychotic DisordersMental Disorders

Study Officials

  • Mehmet Hamdi ÖRÜM, MD, Associate Professor

    Elazığ Mental Health and Diseases Hospital

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor Mehmet Hamdi Örüm, MD, Psychiatrist

Study Record Dates

First Submitted

February 20, 2026

First Posted

February 25, 2026

Study Start

May 1, 2025

Primary Completion

August 31, 2025

Study Completion

August 31, 2025

Last Updated

February 25, 2026

Record last verified: 2026-02

Data Sharing

IPD Sharing
Will share

Deidentified individual participant data (IPD) underlying the results reported in this study (including demographic variables, serum α-N-acetylgalactosaminidase levels, complete blood count parameters, and Positive and Negative Syndrome Scale (PANSS)) will be made available to qualified researchers upon reasonable request for academic purposes. Data will be shared after removal of all direct identifiers and in accordance with applicable ethical approvals and data protection regulations. Access to the data will require a methodologically sound research proposal and a data use agreement. Requests should be directed to the corresponding author.

Shared Documents
STUDY PROTOCOL
Time Frame
Data will be available beginning 6 months after publication and will remain available for 5 years.
Access Criteria
Access will be granted to researchers who provide a methodologically sound proposal. Requests must be approved by the principal investigator and may require a data use agreement in accordance with institutional and ethical regulations.

Locations