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effect of Gemfibrozil for treatment of cigarette

The effect of Gemfibrozil for treatment of cigarette dependence

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017101732057N3
Enrollment
76
Registered
2017-11-01
Start date
2015-08-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

nicotine dependence. Mental and behavioural disorders due to use of tobacco

Interventions

Intervention 1: Control Group: This group receives placebo for seven weeks. Intervention 2: Intervention group: Gemfibrozil 300 mg for twice daily mg for seven weeks.
Treatment - Drugs
Control Group: This group receives placebo for seven weeks
Intervention group: Gemfibrozil 300 mg for twice daily mg for seven weeks

Sponsors

Vice chancellor for research of Kashan University of Medical Sciences and Health Services
Lead Sponsor

Eligibility

Sex/Gender
All
Age
19 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Having an age of 19–65 years; nicotine dependence based on DSM 5; lack of history of psychotic disorders; having negative results in opioid and amphetamines test; lacking diagnosis of chronic disease such as debate, blood pressure , cancer and etc; Not be pregnant. Exclusion criteria: Unwillingness to continue participating in the study; being pregnancy during study; uses drugs with contraindication or Interference with Gemfibrozil such as Anticoagulants, statins, other fibrates and niacin.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Smoking cessation. Timepoint: Before intervention; 1,2,3,4,5,6,7,8,11,14,19 after beginning of intervention. Method of measurement: Expiratory CO2 concentration.;Nicotine dependence. Timepoint: Before intervention; 1,2,3,4,5,6,7,8,11,14,19 after beginning of intervention. Method of measurement: fagestrom nicotine dependence scale.;Nicotine Withdrawal. Timepoint: Before intervention; 1,2,3,4,5,6,7,8,11,14,19 after beginning of intervention. Method of measurement: Minnesota Nicotine Withdrawal Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaohamadreza Davoudi

Kashan University of Medical Sciences and Health Services

msc.davoudi.psy@gmail.comdavoudi-mr@kaums.ac.ir+98 31 5554 9111

Outcome results

None listed

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