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Effect of Rose Essence on sexual dysfunction and happiness

Comparison of Rose Essence and placebo in improving sexual disorders and increase of happiness in men treated with methadone

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015091523705N1
Enrollment
60
Registered
2015-12-15
Start date
2015-09-18
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

Sexual dysfunction. Sexual dysfunction, not caused by organic disorder or disease

Interventions

Intervention 1: In the experimental group, the participants will receive a capsule of rose essence daily ,then the questionnaire will be re-distributed at the baseline, 4 weeks later, and at the end
Treatment - Drugs
Placebo
In the experimental group, the participants will receive a capsule of rose essence daily ,then the questionnaire will be re-distributed at the baseline, 4 weeks later, and at the end of the study (8
In the control group participant will receive a placebo capsule daily. then questionnaire will be redistributed at baseline,4 weeks later, and at the end of the study (8 weeks after the start of the s

Sponsors

Vice chancellor for research, Kermanshah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
20 Years to 48 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients under methadone treatment; elementary education or higher; married; age between 20-48 years; have not sexual problems before treatment with methadone; no history of any glands disease, such as elevated prolactin and thyroid disorder. Exclusion criteria: allergy to products made from rose essence; changes in sexual activity because of (wife pregnancy, remarried, divorce).

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Sexual dysfunction. Timepoint: The beginning of the study (baseline), week four and end of the study (week eight). Method of measurement: Based on sexual function questionnaire (IIEF).;Happiness. Timepoint: The beginning of the study (baseline), week four and end of the study (week eight). Method of measurement: Based on happiness questionnaire(OHI).;Level of the Thyroid hormone. Timepoint: Beginning and end of the study (week eight). Method of measurement: By experimental Kit.;Sexual hormones level. Timepoint: The baseline and end of the study(Eighth week). Method of measurement: By experimental Kit.

Countries

Iran (Islamic Republic of)

Contacts

Public Contact?Dr. Vahid Farnia

Kermanshah University of Medical Sciences

Vfarnia@yahoo.com+98 83 3826 4513

Outcome results

None listed

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