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Clinical Trial for The Wearable Penile Erectile Monitor

Clinical Trial for The Wearable Penile Erectile Monitor

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000030340
Enrollment
Unknown
Registered
2020-02-29
Start date
2020-07-01
Completion date
Unknown
Last updated
2020-03-02

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

Conditions

Erectile dysfunction of penis

Interventions

Gold Standard:Penile erection multi-parameter quantitative analyzer WLYY-2009
Index test:wearable&#32
erection&#32
Hiensor&#32

Sponsors

The University of Hong Kong-Shenzhen Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-55 years; 2. Subjects without mental illness; 3. The penis and its surrounding skin are intact without infection; 4. The subjects had good compliance, agreed to participate in the experiment and signed the informed consent; 5. The subject's mobile phone needs more than 10.0 IOS system, iPhone 6 or Android system's mobile phone needs more than 8.0 Android. The brands are Huawei, Xiaomi, oppo and vivo.

Exclusion criteria

Exclusion criteria: 1. In the past week, I have taken antihypertensive drugs, androgens and psychoactive drugs; 2. Participated in other clinical trials in the last three months; 3. Severe heart, brain, liver and kidney dysfunction; 4. Subjects with a history of silicone allergy; 5. Subjects considered unsuitable for the clinical trial.

Design outcomes

Primary

MeasureTime frame
Consistent rate of effective erections of penis (Kappa);

Countries

China

Contacts

Public ContactJianggen Yang

Shenzhen Luohu People's Hospital (The Third Affiliated Hospital of Shenzhen University)

13392880022@163.com+86 13392880022

Outcome results

None listed

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