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Effect of Levetiracetam on Benzodiazepine Withdrawal Syndrome

Evaluating the Effect of Levetiracetam on Benzodiazepine Withdrawal Syndrome in Comparison with Placebo

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200701047979N1
Enrollment
39
Registered
2020-07-20
Start date
2020-06-28
Completion date
Unknown
Last updated
2020-08-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Benzodiazepine Withdrawal Syndrome. Adverse effect of benzodiazepines

Interventions

Intervention 1: Control group: patients in this group are given placebo 2 times a day for 2 weeks-The placebos are the exact physical replica of Levetiracetam tablets manufactured by Abidi Pharmaceuti

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients who had been taking Benzodiazepines for at least three months, and have not discontinued them for more than one month.

Exclusion criteria

Exclusion criteria: Patients diagnosed with acute and major psychological disorders, schizophrenia, epilepsy, or concurrent neurological disorders, e.g. Multiple Sclerosis Patients with a history of taking Levetiracetam or receiving concurrent Gabapentin or Carbamazepine in the last six months Patients younger than 15 years of age Allergic reactions to Levetiracetam or its excipients Severe adverse drug reactions

Design outcomes

Primary

MeasureTime frame
Sum of Scores for CIWA-B Questionnaire. Timepoint: At benzodiazepine cessation and before taking Levetiracetam, then 2 weeks after taking Levetiracetam. Method of measurement: CIWA-B Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSheida Javid

Tehran University of Medical Sciences

sh.javid@yahoo.com+98 21 8888 7260

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026