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Comparison of Paroxetin Effectiveness Compared to Dupoxitin in Treatment of premature ejaculation Patients

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180512039618N1
Enrollment
110
Registered
2019-04-01
Start date
2639-12-14
Completion date
Unknown
Last updated
2019-04-23

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

Conditions

Premature ejaculation. F52.4

Interventions

Intervention 1: Intervention group: men 19-64 years old with premature ejaculation with paroxetine. Intervention 2: Intervention group: men 19-64 years old with premature ejaculation with Dapoxetine.

Sponsors

Islamic Azad University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
19 Years to 65 Years

Inclusion criteria

Inclusion criteria: Occurrence of intravaginal ejaculatory latency time less than one minute Not receiving other treatments in the past month Male Single sexual partner Patient consent for the measurement of ejaculation time No allergy to paroxetine and dapoxetine and other contraindications Age 19-65

Exclusion criteria

Exclusion criteria: No precocious (premature) ejaculation Azospermia Men without external genitalia Occurrence of cryptorchidism in men Erection inability Homosexual men Use of Viagra Men questioning their gender identity Men having extramarital sex

Design outcomes

Primary

MeasureTime frame
Improve Intravaginal Ejaculatory Latency Time up 1.5 min. Timepoint: Paroxetine: daily for 1 mouth , Dapoxetine: before sex activity. Method of measurement: stop watch.

Secondary

MeasureTime frame
Travaginal Ejaculatory Latency Time. Timepoint: 1 month. Method of measurement: question.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHoessin Keyhan

Islamic Azad University

Sara.hajinajafi@yahoo.com+98 21 3660 4854

Outcome results

None listed

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