With sever ED (subtracting placebo
effect), only 23% and 40% were satisfied for two questions (below). For most
with sever ED the improvement is none or marginal.
Curr Med Res Opin, 2005 Nov;21(11):1701-9
Two question: satisfaction
with intercourse, and enjoyment of intercourse. RESULTS: At least moderate satisfaction (IIEF overall satisfaction domain)
was reported by 55% and 72% of patients with mild ED taking tadalafil 10 mg and 20 mg, respectively, compared with 33% taking
placebo (p < 0.002); 60% and 65% vs. 19% of patients with moderate ED (p < 0.001); and 32% and 49% vs. 9% with severe
ED (p < 0.001). Satisfactory intercourse during most attempts or almost always/always (IIEF-Q7) was reported by 59% and
79% of patients with mild ED taking tadalafil 10 mg and 20 mg vs. 32% taking placebo (p < 0.001); 52% and 65% vs. 18% with
moderate ED (p < 0.001); and 28% and 49% vs. 5% with severe ED (p < 0.001). Highly or very highly enjoyable intercourse
(IIEF-Q8) was reported by 45% and 63% of patients with mild ED taking tadalafil 10 mg and 20 mg vs. 21% taking placebo (p
< 0.001); 43% and 56% vs. 16% with moderate ED (p < 0.001); and 19% and 44% vs. 5% with severe ED (p < 0.001). CONCLUSIONS:
Compared with placebo, tadalafil 10 mg and 20 mg improved overall satisfaction with the sexual experience, intercourse satisfaction,
and intercourse enjoyment in men with mild, moderate, and severe ED.
Urology, 2002 Sep;60(2 Suppl 2):12-27.
The efficacy
of sildenafil citrate (Viagra) in clinical populations: an update.
Carson CC., Burnett AL, et al
{a meta study} Efficacy evaluations included the International Index of Erectile Function, a global efficacy
question ("Did treatment improve your erections?"), and a patient-recorded event log of sexual activity. Significantly improved
erectile function was demonstrated for sildenafil compared with placebo for all efficacy parameters analyzed (P <0.02 to
0.0001), regardless of patient age, race, body mass index, ED etiology, ED severity, ED duration, or the presence of various
comorbidities. Long-term effectiveness was assessed in 3 open-label extension studies.
Of those who continued long-term therapy (1 to 3 years) with sildenafil, >95% of patients reported that they were
satisfied with the effect of treatment on their erections, and that treatment had improved their ability to engage in sexual
activity
Erectile function and assessments of erection
hardness correlate positively with measures of emotional well-being, sexual satisfaction, and treatment satisfaction in men
with erectile dysfunction treated with sildenafil citrate (Viagra).
Urology. 2006 Sep;68(3 Suppl):26-37. Review.
PMID: 17011373 [PubMed - indexed for MEDLINE]
Curr Med Res Opin 2006
May;22(5):939-48.
Correlation of improved
erectile function and rate of successful intercourse with improved emotional well-being assessed with the Self-Esteem And
Relationship questionnaire in men treated with sildenafil for erectile dysfunction and stratified by age. The psychosocial measures of well-being
assessed with the SEAR were positively correlated (range 0.60-0.86, P < 0.0001) with erectile function, the frequency of
achieving erections that allowed satisfactory sexual intercourse, the percentage of successful sexual intercourse attempts,
and global treatment efficacy.
Urol, 2006 Mar;175(3 Pt 1):1058-62.
Erectile Function domain
scores (r range 0.34 to 0.69, p < 0.0001), other IIEF domain scores (p < 0.0001), percentage of successful intercourse
attempts (p < 0.0001) and frequency of erection that allowed satisfactory intercourse (p < 0.0001).
Urology, 2006 Sep;68(3 Suppl):17-25
Pooled data from 6549
men with ED provided strong proof and improved characterization of the response to sildenafil. Almost half of men with ED
and a baseline IIEF EF domain score classified as "severe ED" (< or = 10) shifted to a score classified as "no ED" (>
or = 26). Sildenafil recipients showed greater mean improvement from baseline to end point in IIEF Q2 scores versus placebo,
regardless of baseline ED severity, and a higher mean percentage of successful sexual intercourse attempts occurred during
the last 4 weeks of treatment versus placebo (5.4-fold vs 2.0-fold increase from baseline). At end point, 95% of men who scored
"no ED" on the IIEF EF domain and 92% of men who reported "almost always/always" achieving an erection hard enough for penetration
(IIEF Q2) had graded their erections hard (rigid) enough for penetration (grade 3) or completely hard and fully rigid (grade
4) during the last 4 weeks of treatment,
With sever ED (subtracting placebo
effect), only 23% and 40% were satisfied for two questions (below). For most
with sever ED the improvement is none or marginal.
Curr Med Res Opin, 2005 Nov;21(11):1701-9
Two question: satisfaction
with intercourse, and enjoyment of intercourse. RESULTS: At least moderate satisfaction (IIEF overall satisfaction domain)
was reported by 55% and 72% of patients with mild ED taking tadalafil 10 mg and 20 mg, respectively, compared with 33% taking
placebo (p < 0.002); 60% and 65% vs. 19% of patients with moderate ED (p < 0.001); and 32% and 49% vs. 9% with severe
ED (p < 0.001). Satisfactory intercourse during most attempts or almost always/always (IIEF-Q7) was reported by 59% and
79% of patients with mild ED taking tadalafil 10 mg and 20 mg vs. 32% taking placebo (p < 0.001); 52% and 65% vs. 18% with
moderate ED (p < 0.001); and 28% and 49% vs. 5% with severe ED (p < 0.001). Highly or very highly enjoyable intercourse
(IIEF-Q8) was reported by 45% and 63% of patients with mild ED taking tadalafil 10 mg and 20 mg vs. 21% taking placebo (p
< 0.001); 43% and 56% vs. 16% with moderate ED (p < 0.001); and 19% and 44% vs. 5% with severe ED (p < 0.001). CONCLUSIONS:
Compared with placebo, tadalafil 10 mg and 20 mg improved overall satisfaction with the sexual experience, intercourse satisfaction,
and intercourse enjoyment in men with mild, moderate, and severe ED.
85% satisfied compared to 46% for placebo
Eur Urol, 2004 Sep;46(3):362-9; discussion 369
RESULTS: Of the 443 men
who entered the trial, 409 (mean age, 52 years) formed the intent-to-treat population. Mean baseline demographics and ED severity
measures were balanced between treatment groups except for a higher percentage of patients naive to sildenafil in the tadalafil
group compared to placebo (50% versus 36%). EDITS score of 84
(95%CI 80, 86), which was significantly higher than the median score for placebo-treated patients of 41 (95%CI 32, 59; p <
0.001; Wilcoxon test). The proportion of patients satisfied with treatment (defined as final EDITS score greater than 50)
was 87% for the tadalafil-treated group and 46% for the placebo-treated group (p < 0.001; exact test).