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A Real World Research: Comparison of Precision and Experience Therapy for Hypertension, Diabetes or Hyperlipidemias

Real World Research Based on Genomics: Comparison of Precision and Experience Therapy for Chronic Cardiovascular and Cerebrovascular Diseases

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04660630
Acronym
RCG
Enrollment
1172
Registered
2020-12-09
Start date
2020-01-21
Completion date
2025-01-20
Last updated
2020-12-09

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

Conditions

Diabetes type2, Hyperlipidemias, Hypertension,Essential

Brief summary

The purpose of this study is to evaluate the effectiveness, safety and health economics of precise drug use strategies based on pharmacogenomics compared with traditional drug use strategies for cardiovascular related chronic diseases.

Detailed description

This study is a randomized controlled, single blind, multicenter clinical study. Beijing Chaoyang Hospital is the team leader, and director Liu Lihong is the project leader. The sub center is Daming County Street Town Health Center and Daming County Jiuzhi township health center. The team leader is responsible for the formulation, implementation and coordination of the research plan, and each sub center is responsible for the implementation of the specific study, patient management and research information feedback. Three project groups were set up in this study: primary hypertension, type 2 diabetes and hyperlipidemia. In each group, the control group and the experimental group were set up, and the patients in two pilot towns of Daming County were selected by cluster stratified random sampling. The control group received the treatment of local researchers according to the traditional medication strategy. The patients in the experimental group were treated with the drug regimen formulated by local researchers according to the results of their pharmacogenomic test reports. The subjects were single blind.

Interventions

DIAGNOSTIC_TESTGene detection of therapeutic drugs for chronic cardiovascular and cerebrovascular diseases

According to the results of drug gene chip detection, we combined with the clinical characteristics of the patient to choose more suitable cardiovascular and cerebrovascular treatment drugs.

BEHAVIORALRegular follow-up and patient education

The subjects received regular follow-up and patient education.

Sponsors

China development research foundation
CollaboratorUNKNOWN
Beijing Chao Yang Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
55 Years to 120 Years
Healthy volunteers
No

Inclusion criteria

1. They are 55 years old or above, with no gender restriction. They are permanent residents of Da-jie town and Jiu-zhi Township in Da-ming County. 2. Patients who meet one of the following: A. Hypertension project group: Primary hypertension was definitely diagnosed, systolic blood pressure ≥ 140 millimeter of mercury, diastolic blood pressure ≥ 90 millimeter of mercury, or both after drug treatment. B.Type 2 Diabetes project group: Patients with type 2 diabetes mellitus (non insulin dependent diabetes mellitus) who were diagnosed as type 2 diabetes mellitus (NIDDM) and had HbA1c ≥ 7.0% after drug treatment before enrollment. C.Hyperlipidemia project group: Those who were diagnosed as hyperlipidemia and were treated with or without medication before enrollment. 3. Patients who can provide real and reliable information related to drug treatment and efficacy evaluation

Exclusion criteria

1. Respondents who are not willing to fill in the true and reliable information form for any reason. 2. Patients with infectious diseases or serious life-threatening diseases such as malignant tumors. 3. Patients with severe liver and kidney function damage, affecting the choice of treatment drugs. 4. Patients with incomplete data related to study evaluation such as any of following: A.The clinical data did not include systolic blood pressure, diastolic blood pressure, heart rate, glycosylated hemoglobin, fasting blood glucose, total cholesterol, low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, triglyceride core efficacy evaluation indicators. B.The data related to adverse reactions required by clinical research can not be collected, including but not limited to the related drugs with adverse reactions, adverse reaction performance, time correlation, whether to stop suspicious drugs, and whether to stimulate adverse reactions by re-medication. C.The information of medication compliance score and quality of life score could not be provided for any reason.

Design outcomes

Primary

MeasureTime frameDescription
change of systolic pressure3 monthsChange of systolic blood pressure from baseline
change of triglyceride3 monthsChange of triglyceride from baseline
change of low density lipoprotein cholesterol3 monthsChange of low density lipoprotein cholesterol from baseline
change of total cholesterol3 monthsChange of total cholesterol from baseline
change of fasting blood glucose3 monthsChange of fasting blood glucose from baseline
change of glycosylated hemoglobin3 monthsChange of glycosylated hemoglobin from baseline
change of diastolic pressure3 monthsChange of diastolic blood pressure from baseline

Secondary

MeasureTime frameDescription
Compliance rate of glycosylated hemoglobin12 monthsChange of the compliance rate of glycosylated hemoglobin from baseline
Compliance rate of blood pressure12 monthsChange of the compliance rate of blood pressure from baseline
Compliance rate of low density lipoprotein cholesterol12 monthsChange of the compliance rate of low density lipoprotein cholesterol from baseline

Other

MeasureTime frameDescription
Change of the medicine costs of hypertension treatment12 monthsChange of annualized cost of hypertension treatment from baseline.
Health self assessment12 monthsChange of the score of EuroQol five dimensions questionnaire from baseline.
Medication compliance12 monthsChange of the score of Morisky Medication Adherence Scale(MMAS-8) from baseline.
Change of the medicine costs of hyperlipidemia treatment12 monthsChange of annualized cost of hyperlipidemia treatment from baseline.
Change of the total costs of hyperlipidemia treatment12 monthsChange of annualized cost of hyperlipidemia treatment from baseline.
change of the medicine costs of diabetes treatment12 monthsChange of annualized cost of diabetes treatment from baseline.
Change of the total costs of diabetes treatment12 monthsChange of annualized cost of diabetes treatment from baseline.
Change of the total costs of hypertension treatment12 monthsChange of annualized cost of hypertension treatment from baseline.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026