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Evaluation of the role of Atorvastatin to improve the response to Sildenafil in men with erectile dysfunction without response to Sildenafil alone

Evaluation of the role of Atorvastatin to improve the response to Sildenafil in men with erectile dysfunction without response to Sildenafil alone

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT138802301267N3
Enrollment
152
Registered
2009-08-03
Start date
2009-06-22
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

Erectile dysfunction. Impotence of organic origin

Interventions

Intervention 1: Atorvastatin 40 mg/day and Sildenafil 100 mg before every intercourse. Intervention 2: Placebo with the same dose and shaoe as Atorvastatin and Sildenafil 100 mg before every intercour
Treatment - Drugs
Atorvastatin 40 mg/day and Sildenafil 100 mg before every intercourse
Placebo with the same dose and shaoe as Atorvastatin and Sildenafil 100 mg before every intercourse

Sponsors

Urology and Nephrology Research Center ( UNRC), Shahid Beheshti University, M.C.( SBMU), Tehran
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: Inclusion criteria: Presence of erectile dysfunction and without a proper response to the Sildenafil treatment, Exclusion criteria: Receiving nitrate drugs, high serum lipids (LDL>130, Cholestrol >200), Receiving Statin drugs, Acute coronary accidents in the 6 month prior to study, severe and uncontrolled diabetes mellitus, active thyroid disease, mental disorder or depression diagnosed by a psychiatrist, prostate surgery history with the consequent ED, active liver disease, renal failure (cr>2)

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Erectile dysfunction. Timepoint: Baseline and 6 and 12 weeks after treatment. Method of measurement: IIEF-5 questionnaire.

Secondary

MeasureTime frame
Sexual ability. Timepoint: Baseline and 6 and 12 weeks after treatment. Method of measurement: IIEF-5 ? GEQ questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Alireza Lasheie

Urology and Nephrology Research Center ( UNRC), Shahid Beheshti University, M.C.( SBMU), Tehran, I.R

Research@unrc.ir+98 22567222

Outcome results

None listed

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