Status:
UNKNOWN
Observational Study of Pharmacological Treatment for Premature Ejaculation Concurrent With Erectile Dysfunction
Lead Sponsor:
Yan-Ping Huang
Conditions:
Premature Ejaculation
Erectile Dysfunction
Eligibility:
MALE
18-60 years
Phase:
PHASE3
Brief Summary
Premature ejaculation (PE) is a common disease in the andrology clinic. Currently, the effectiveness and outcome differences of drug treatment still need to be studied and demonstrated. Premature ejac...
Eligibility Criteria
Inclusion
- PE concurrent with ED: the IELT is less than 3 minutes, the PEDT score is ≥11 points, and 5≤IIEF-5≤21 points.
- 18-60 years old, outpatient or physical examination population, with regular sex partners and regular sex life;
- Having the data below,and willing to participate in the trial（1）Demographic information: age, gender, nationality, birthplace, etc;(2) Physical examination data: height, weight, abdominal circumference, blood pressure, heart rate, etc ;(3) Medical history data: history of present illness, past medical history, family history, etc;(4) Scale evaluation: Premature Ejaculation Diagnostic Tool (PEDT), Premature Ejaculation Profile (PEP), International Erectile Function Score-5(IIEF-5), Erectile Hardness Grading Score (EHGS), Clinical Global Impression of Change (GICC);
Exclusion
- Age \<18 years or\> 60 years;
- There is a history of acute and chronic diseases, major trauma and surgery, etc;
- A long history of medication;
- There is a history of unstable myocardial infarction and cerebral infarction;
- A history of cardiogenic shock, severe heart failure, severe ventricular arrhythmia, etc;
- There are serious diseases such as malignant tumors, chronic liver and kidney diseases, etc.
Key Trial Info
Start Date :
June 3 2020
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
April 1 2021
Estimated Enrollment :
150 Patients enrolled
Trial Details
Trial ID
NCT04361305
Start Date
June 3 2020
End Date
April 1 2021
Last Update
April 24 2020
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