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A correlative study of the effect of allisartan isoproxil on sexual function and nocturnal blood pressure in male patients with mild to moderate hypertension

A correlative study of the effect of allisartan isoproxil on sexual function and nocturnal blood pressure in male patients with mild to moderate hypertension

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500106035
Enrollment
Unknown
Registered
2025-07-16
Start date
2022-09-05
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Hypertension

Interventions

Groups A+C:allisartan isoproxil tablets 240mg in combination with amlodipine benzenesulfonate tablets 5mg
Groups A+B:given allisartan isoproxil tablets 240mg in combination with metoprolol succinate extended-release tablets 47.5mg for 6 months.

Sponsors

Lanzhou University Second Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1 Male, aged 18 to 75 years; 2 Patients with grade 1 or 2 essential hypertension diagnosed according to the Chinese Guidelines for the Prevention and Control of Hypertension, 2018 Revision; 3 A stable sexual partner who has been having sex (at least 1 sexual intercourse every 3 to 5 d.). ; 4 All enrolled individuals voluntarily signed an informed consent form.

Exclusion criteria

Exclusion criteria: 1 Secondary hypertension; 2 Hypertensive emergencies, coronary artery heart disease (coronary heart disease), heart valve disease, bradycardia (heart rate <45 beats/min), degree II or degree III atrioventricular block, sick sinus node syndrome, severe peripheral vascular disease, cardiac function class II and above; history of cerebrovascular accident, multiple sclerosis, epilepsy, Parkinson's disease, stroke, Alzheimer's disease and spinal cord injury Diabetes mellitus, severe hepatic or renal insufficiency, thyroid disease; genitourinary surgery, abnormal sexual development, abnormal sex hormone secretion; continuous use of nafil analogues for more than 4 weeks prior to enrollment, history of severe psychiatric illnesses, history of alcohol or drug abuse, and serious conflicts with their sexual partners; 3 Known or suspected allergy to active or inactive components of the study medication; 4 Patients refusing to answer the questions, fill out the form, or take blood; 5 Patients unwilling to participate in this study. Patients;

Design outcomes

Primary

MeasureTime frame
Sexual function score;blood pressure;

Countries

China

Contacts

Public ContactJing Yu

Lanzhou University Second Hospital

2550372204@qq.com+86 189 5841 8389

Outcome results

None listed

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