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The Pharmacological Basis for the Increase in Visual Time Constants Induced by Single Oral Doses of Sildenafil

The Pharmacological Basis for the Increase in Visual Time Constants Induced by Single Oral Doses of Sildenafil

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00463957
Enrollment
12
Registered
2007-04-20
Start date
2006-08-31
Completion date
Unknown
Last updated
2010-01-12

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

Conditions

Erectile Dysfunction

Keywords

sildenafil, tadalafil, phosphodiesterase, visual persistence, reaction time

Brief summary

Sildenafil and similar drugs have been used for several years to treat erectile dysfunction. It has been noticed that in some people, sildenafil causes a subtle increase in the length of time that visual images that we see are retained by the retina. It is thought that this might be due to an effect of sildenafil on inhibiting an enzyme called phosphodiesterase type 6 (PDE6) which is present in the retina. By giving single oral doses of sildenafil and a similar drug called tadalafil which has less effect on PDE6, we hypothesise that this is the mechanism of the change in vision caused by sildenafil. By performing computerised visual test, we plan to compare the effects of sildenafil, tadalafil and placebo tablets on vision in healthy volunteers.

Interventions

DRUGsildenafil
DRUGtadalafil
DRUGplacebo

Sponsors

University of Cambridge
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
DOUBLE

Eligibility

Sex/Gender
MALE
Age
18 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy * Male * 18-55 years

Exclusion criteria

* Significant medical or psychiatric illness * Cardiac disease * Hyper or hypotension * Renal disease * Liver disease * Stroke * Sickle cell anaemia * Multiple myeloma * Leukaemia * Bleeding disorders * Peyronie's disease * Priapism * Subjects receiving prescribed medications * Subjects with known visual abnormalities other than refractive errors, including retinitis pigmentosa, optic neuropathy

Design outcomes

Primary

MeasureTime frame
visual persistence
reaction time

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026