Skip to content

Clinical application research on the intelligent improvement of the MSIEDY system for assessing the etiology and structure of erectile dysfunction

Clinical application research on the intelligent improvement of the MSIEDY system for assessing the etiology and structure of erectile dysfunction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400093688
Enrollment
Unknown
Registered
2024-12-10
Start date
2025-01-01
Completion date
Unknown
Last updated
2024-12-16

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

Conditions

Erectile Dysfunction

Interventions

Regular consultation:Diagnosis and treatment of enrolled patients using standard inquiry methods
Intelligent improvement of the etiology and structural assessment system for erectile dysfunction:Diagnosis and treatment of patients with erectile dysfunction using an intelligent improved etiology a

Sponsors

Xiangya Hospital,Central South Univerity
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) 20 <= Age <= 60 years old, (2) Patients clinically diagnosed with erectile dysfunction; (3) International Index of Erectile Function score (IIEF-5) <= 21 points; (4) Having a fixed sexual partner and normal sexual desire; (5) Voluntarily sign an informed consent form before the start of activities related to this trial, understand the procedures and methods of this trial, and be willing to strictly follow the clinical trial protocol to complete this trial.

Exclusion criteria

Exclusion criteria: (1) Asexual life; (2) Complicated with urethritis, acute prostatitis, diabetes; (3) Individuals with abnormal development of internal and external genitalia; (4) Patients with other serious systemic diseases, such as severe cardiovascular and cerebrovascular diseases, liver and kidney dysfunction, hematological disorders, mental illnesses, malignant tumors, etc; (5) Patients with poor compliance, failure to receive treatment as prescribed, or mental or consciousness disorders that prevent them from cooperating with treatment independently; (6) Patients with erectile dysfunction or organic erectile dysfunction caused by traumatic penile injury; (7) Long term use of drugs that affect sexual function in patients; (8) In addition to the above, the researchers have determined that patients who are not suitable to participate in this clinical trial.

Design outcomes

Primary

MeasureTime frame
Accuracy;Specificity;Youden Index;Kappa;Patient visit time;patient satisfaction;

Countries

China

Contacts

Public ContactDongjie Li

Xiangya Hospital,Central South Univerity

dongjieli@csu.edu.cn+86 137 5501 1481

Outcome results

None listed

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