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Study for erectile dysfunction in Chinese population

Study for erectile dysfunction in Chinese population

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900025700
Enrollment
Unknown
Registered
2019-09-05
Start date
2019-01-01
Completion date
Unknown
Last updated
2019-09-09

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

Conditions

erectile dysfunction

Interventions

Case series:Nil

Sponsors

The Fifth Hospital Affiliated to Zhongshan University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Aged 18-80 years male; (2) Agree to participate in this clinical study and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Any unstable medical, psychiatric, spinal cord injury, abnormal penile anatomy, pre-test diagnosis of gonadal dysplasia (primary and secondary); 2. Use anti-androgen and/or GnRH agonist drugs before the test, as well as patients who use spironolactone, antipsychotics, antidepressants, antiepileptics or immunosuppressive drugs; 3. Currently involved in other clinical studies; 4, Refuse to sign informed consent.

Design outcomes

Primary

MeasureTime frame
uric acid;Color ultrasound examination;Pepsinogen;Glycosylated hemoglobin;—

Secondary

MeasureTime frame
glucose;RBC, WBC, NEUT, HGB, PLT;Height;Weight;waist;Hipline;Waist-hip ratio;PSA;AFP;Cholesterol;triglyceride;HDL-c;LDL-c;blood pressure;ca-199;Vasodilation rate;—

Countries

China

Contacts

Public ContactYuxin Tang

The Fifth Hospital Affiliated to Zhongshan University

mmcct@126.com+86 18125075933

Outcome results

None listed

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