Sexual dysfunction. Sexual dysfunction not due to a substance or known physiological condition
Conditions
Interventions
Intervention 1: Intervention group: after justifying the patients and providing the necessary training, 75 mg bupropion tablets are prescribed once a day during the study (8 weeks). Intervention 2: Co
Sponsors
Tabriz University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
15 Years to 55 Years
Inclusion criteria
Inclusion criteria: Patients under SSRI treatment for at least three consecutive months; having sexual dysfunction for at least the last two months; married and sexually active; Age range 15-55 years; stable vital signs.
Exclusion criteria
Exclusion criteria: The presence of digestive problems such as severe nausea and vomiting and SSRI intolerance; The presence of concurrent chronic liver or kidney disease; The presence of any anatomical problem of the reproductive system; The existence of any severe or relatively severe hormonal disorder; Absence of pregnancy; Lack of breastfeeding; Non-participation in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Measuring sexual satisfaction. Timepoint: Once a Month. Method of measurement: Hudson's Standardized Sexual Satisfaction Questionnaire (ISS).;Measuring sexual performance. Timepoint: Once a Month. Method of measurement: Rozen Standardized Women's Sexual Performance Questionnaire (FSFI). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Elham Ghasemi
Tabriz University of Medical Sciences
Outcome results
None listed