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A multi-center prospective randomized clinical research about erectile dysfunction-no sexual life

A multi-center prospective randomized clinical research about erectile dysfunction-no sexual life

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-12002039
Enrollment
Unknown
Registered
2012-03-25
Start date
2011-07-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

The asexual erectile dysfunction

Interventions

Blank control group:Psychological counseling * 12W
Treatment group:Tadalafil (5mg, qn*12W)
The placebo group:Tadalafil (5mg, qn*12W)

Sponsors

The First Affiliated Hospital of Wenzhou Medical College
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
16 Years to 50 Years

Inclusion criteria

Inclusion criteria: Asexual life for more than six months;Normal sexual desire; Feel that decline in erectile hardness, shorten the time and lack of erection confidence and can not try the sex life.

Exclusion criteria

Exclusion criteria: Diabetes, hypertension, metabolic syndrome and other serious medical illness; History of pelvic surgery or within 6 months of surgery; Serious neurological or psychiatric disorders; Peyronie organic penis diseases and all kinds of penis with congenital malformations, etc. Blood test,liver and kidney function, blood lipids, fasting glucose, sex hormone (PRL, T, E2,LH, FSH) was significantly abnormal in patients.

Design outcomes

Primary

MeasureTime frame
Liver and kidney function;blood lipids;Blood test;fasting glucose;Sex hormone series;EDNA questionnaire;CPSI score;Psychological self-assessment;Erectile hardness classification;Urinary flow rate;

Countries

China

Contacts

Public ContactZhigang Wu
wzg8141@163.com+86 13676467276

Outcome results

None listed

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