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IRCT2016062523705N5 IRCT 2016-07-11 Vice chancellor for research, Kermanshah University of Medical Sciences Effect of Ginseng on sexual performance status in men and women Comparison of Ginseng and placebo on sexual performance status in men and women treated with methadone 2016-07-22 anticipated 70 Complete https://irct.ir/trial/20211 interventional Randomization: Randomized, Blinding: Double blinded, Placebo: Used, Assignment: Parallel, Purpose: Treatment. N/A Sexual dysfunction. Intervention 1: In the experimental group, the participants will receive four capsules of Ginseng daily ,then the questionnaire will be re-distributed at the baseline and at the end of the study (4 weeks after the start of the study), and sexual function will be measured. Intervention 2: In the control group participant will receive four placebo capsules daily. then questionnaire will be redistributed at baseline and at the end of the study (4 weeks after the start of the study), and sexual function will be measured.
public Dr. Vahid Farnia
Farabi Hospital, Isar square
Kermanshah Iran (Islamic Republic of) +98 83 3826 4513 vfarnia@yahoo.com Kermanshah University of Medical Sciences scientific Dr. Alireza Ebrahimi
Farabi Hospital, Isar square
Kermanshah Iran (Islamic Republic of) +98 83 3826 4513 alirezaebrahimi1344@yahoo.com Kermanshah University of Medical Sciences Iran (Islamic Republic of) Inclusion criteria: patients undergoing methadone treatment; married; age between 18-50 years; lack of sexual problems before treatment with methadone. Exclusion criteria: Under age of 18, drugs that positive and negative affect on sexual performance, recent use any other drugs or alcohol, spinal cord injury, radical prostatectomy, singular, the existence of recent mental disorder, recent communication disorder with wife, allergy to Ginseng. 18 years 50 years Both F52 Sexual dysfunction, not caused by organic disorder or disease Treatment - Drugs Placebo In the experimental group, the participants will receive four capsules of Ginseng daily ,then the questionnaire will be re-distributed at the baseline and at the end of the study (4 weeks after the start of the study), and sexual function will be measured In the control group participant will receive four placebo capsules daily. then questionnaire will be redistributed at baseline and at the end of the study (4 weeks after the start of the study), and sexual function will be measured. Sexual dysfunction. Timepoint: The beginning of the study (baseline) and end of the study (week four). Method of measurement: Based on sexual function questionnaire (IIEF) for men and sexual function questionnaire (FSFI ) for women. Vice chancellor for research, Kermanshah University of Medical Sciences Approved 2016-06-08 Ethics committee of Kermanshah University of Medical Sciences Building No.2, Shahid Beheshti, Vice Chancellor for Research Affairs, Kermanshah University of Medical Sciences Kermanshah Iran (Islamic Republic of)