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A prospective study on the effect of Sacubitril Valsartan Sodium in treatment of type 2 diabetes mellitus complicated with hypertension on insulin resistance

A prospective study on the effect of Sacubitril Valsartan in treatment of type 2 diabetes mellitus complicated with hypertension on insulin resistance

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400088532
Enrollment
Unknown
Registered
2024-08-20
Start date
2024-08-20
Completion date
Unknown
Last updated
2024-08-26

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

Conditions

Type 2 diabetes mellitus complicated with hypertension

Interventions

Amlodipine Group:Amlodipine therapy
Sacubitril Valsartan Group:Sacubitril Valsartan therapy

Sponsors

Armed Police Hospital of Chongqing
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: Selection criteria (all 5 must be met): 1. Patients who have been diagnosed as T2DM according to the diagnostic criteria of WHO in 1999. 2. Patients with grade 1-2 essential hypertension. 3. Age = 18 years old. 4. 19 kg/m2 = BMI = 30kg/m2. 5. Be able to understand the procedures and methods of this trial, be willing to strictly abide by the clinical trial plan to complete this trial, and sign the informed consent form.

Exclusion criteria

Exclusion criteria: Exclusion criteria (1 of which is excluded): 1. Secondary hypertension or other types of diabetes. 2.Pregnant and lactating women. 3. Acute complications of severe diabetes mellitus. 4. Patients with severe hepatic and renal insufficiency. 5. Acute attack of severe cardio-cerebrovascular disease. 6. Previous use of insulin sensitizers, GLP-1 or DPP- IV inhibitors, ACEI, ARB or CCB antihypertensive drugs, glucocorticoids and other drugs that have effects on blood sugar. 7. The researchers believe that there are any other circumstances that may prevent the subjects from completing the study or pose a significant risk to the subjects.

Design outcomes

Primary

MeasureTime frame
HOMA-IR;Glycosylated hemoglobin,HbA1c;

Countries

China

Contacts

Public Contactyin jingxia

Armed Police Hospital of Chongqing

906802276@qq.com+86 135 2734 9863

Outcome results

None listed

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