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Clinical observation for Sacubitril Valsartan Sodium in the treatment of refractory hypertension

Clinical observation for Sacubitril Valsartan Sodium in the treatment of refractory hypertension

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000038938
Enrollment
Unknown
Registered
2020-10-10
Start date
2020-10-09
Completion date
Unknown
Last updated
2021-02-16

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

Conditions

Hypertension

Interventions

Treatment plan 1:Valsartan 80mg
Treatment plan 2:Sacubitril Valsartan Sodium 100mg
Treatment plan 3:Sacubitril Valsartan Sodium 200mg

Sponsors

Putuo Hospital, Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 18-80 were diagnosed resistant hypertension; 2. Patients taking 3 or more antihypertensive medications, including one diuretic, who have not yet achieved blood pressure control (> 140/90 mmHg) are referred to as Resistant Hypertension; 3. Signed informed consent.

Exclusion criteria

Exclusion criteria: (1) Secondary hypertension; (2) Patients who had a history of renal artery stenosis or imaging suggestive of renal artery stenosisGFR <45 ml/min /1.73 m2;; (3) Severe liver function damage (Child - Pugh, C); (4) Patients with type 2 diabetes are taking Alighiren; (5) Known existence ACEI or ARB treatment of patients with a history of angioedema always; (6) Genetic or patients with idiopathic angioedema; (7) Pregnant or planning to become pregnant during the study.

Design outcomes

Primary

MeasureTime frame
office blood pressure;ambulatory blood pressure;

Countries

China

Contacts

Public ContactLyu Tianjiao

Department of Cardiology, Putuo Hospital, Shanghai University of Traditional Chinese Medicine

claire925@163.com+86 13917117609

Outcome results

None listed

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