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the efficacy of tramadol in the treatment of premature ejaculation

a comparative study tramadol and sertraline in delaying ejaculation in men with premature ejaculation

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201105236564N1
Enrollment
60
Registered
2011-06-26
Start date
2011-03-21
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

premature ejaculation. The inability to control ejaculation sufficiently for both partners to enjoy sexual interaction

Interventions

interventional group : 50 mg tramadol 3 hours before intercourse for 8 weeks.
Intervention 1: interventional group : 50 mg tramadol 3 hours before intercourse for 8 weeks. Intervention 2: control group : 50 mg sertraline 3 hours before intercourse for 8 weeks.
Treatment - Drugs
control group : 50 mg sertraline 3 hours before intercourse for 8 weeks

Sponsors

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

Eligibility

Sex/Gender
Male
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: inclusion criteria:The married men with lifelong premature ejaculation that intra vaginal ejaculation latency time was < 2 minutes . exclusion criteria : Another erectile dysfunction ; consumption of anti depressant and anti psychotic drugs and secondary premature ejaculation .

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Latency time of ejaculation. Timepoint: after each intercourse. Method of measurement: stop watch.

Secondary

MeasureTime frame
Degree of satisfaction. Timepoint: after each intercourse. Method of measurement: according to questioner.;Control of ejaculation. Timepoint: After each intercourse. Method of measurement: According to questioner.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Mahmood Reza Moradi

Kermanshah University Of Medical Sciences

drmrmoradi@yahoo.com--+98 83 1427 6301

Outcome results

None listed

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