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Aspirin in the treatment of sexual dysfunction

Evaluation of Aspirin efficacy in prevention of erectile dysfunction due to lithium administration in comparison with placebo

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT138711131556N4
Enrollment
40
Registered
2009-02-12
Start date
2009-02-20
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: Asprin (80 mg TDS) as intervention group. Intervention 2: Tab Placebo as control group.
Treatment - Drugs
Asprin (80 mg TDS) as intervention group
Tab Placebo as control group

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
20 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Remission phase of bipolar disorder, maintenance on lithium, sexual dysfunction based on international index of erectile function. Exclusion Criteria: Other psychiatric comorbidity, substance dependence, GI bleeding.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Score of international index of erectile function. Timepoint: every two week. Method of measurement: use of international index of erectile function.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

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