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A real world study to evaluat the efficacy of Beifanluoer on sexual function in young and middle-aged men with hypertension

A real world study to evaluat the efficacy of Beifanluoer on sexual function in young and middle-aged men with hypertension

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200062201
Enrollment
Unknown
Registered
2022-07-29
Start date
2022-07-29
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Hypertension

Interventions

Experimental group:Bevanolol hydrochloride tablets

Sponsors

The First Affiliated Hospital of He'nan University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
30 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Male patients initially diagnosed with grade I-II essential hypertension according to the Diagnostic Criteria of the Chinese Guidelines for Hypertension Prevention and Treatment (2018 Revision); 2. Patients with essential hypertension requiring drug intervention; 3. Aged 30-65 years; 4. Married or cohabitant, with a fixed partner and relatively fixed frequency of sex; 5. There was no obvious clinical manifestation of erectile dysfunction (ED) before treatment; 6. The informed consent has been signed.

Exclusion criteria

Exclusion criteria: 1. Patients who had taken ED drugs before enrollment or planned to take them during the study; 2. Patients with abnormal development of external genitalia and anatomical malformations; 3. Previous history of spinal cord trauma, or other nerve injury or disease affecting sexual function; 4. Patients with uncontrolled diabetes or unstable blood sugar or diabetes complications; 5. Sequelae of cerebrovascular disease, severe cardiovascular diseases (such as cardiogenic shock, cardiac insufficiency, unstable angina, coronary syndrome, myocardial infarction, severe sinus bradycardia, Grade II type II and grade III atrioventricular block), pheochromocytoma, severe lung disease, pulmonary heart disease, hyperlipidemia, patients who have mental or psychological illness or need to be treated with other drugs; 6. Patients with abnormal liver and kidney function; The researcher considered that the patients were not suitable to participate in this study.

Design outcomes

Primary

MeasureTime frame
Changes of International Erectile Function Scale (IIEF-5) scores before and after treatment;

Secondary

MeasureTime frame
Incidence of erectile dysfunction (ED);Effective rate of blood pressure control before and after treatment;

Countries

China

Contacts

Public ContactLiu Xincan

The First Affiliated Hospital of He'nan University of Chinese Medicine

liuxincan103@163.com+86 13203825657

Outcome results

None listed

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