None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) Meet the above diagnostic criteria;(2) Disease duration = 3 months, with an IIEF score between 8-21;(3) Aged 20-55 years old;(4) Having a fixed sexual partner for more than 3 months;(5) No treatment related to this disease received within 4 weeks prior to enrollment;(6) Patients with normal or decreased serum testosterone levels;(7) Patients with good compliance, willingness to participate in the trial, and who sign the informed consent form.
Exclusion criteria
Exclusion criteria: (1) Patients who do not meet the aforementioned diagnostic criteria and inclusion criteria;(2) Patients with severe cardio-cerebrovascular diseases (such as myocardial infarction, arrhythmia, cerebral hemorrhage) as well as severe liver, kidney, hematological, endocrine, or mental illnesses within the past six months;(3) Patients with hypotension or severe hypertension (blood pressure 170/100 mmHg);(4) Patients with erectile dysfunction caused by medications, surgery, trauma, congenital or acquired organic lesions of the penis;(5) Patients who require long-term use of or are currently taking nitrates;(6) Patients whose spouses have severe organic lesions and cannot fully cooperate;(7) Patients allergic to the medications used in this study;(8) Patients with poor compliance, making it difficult to assess therapeutic efficacy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Infrared Thermography Values of Observation Points at Body Surface Acupoints; | — |
Secondary
| Measure | Time frame |
|---|---|
| Serum Testosterone;International Index of Erectile Function;Self-rating Depression Scale;Self-ratingAnxiety Scale; | — |
Countries
China
Contacts
The First Affiliated Hospital of Guizhou University of Traditional Chinese Medicine