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| Name | Class |
|---|---|
| Peking University People's Hospital | OTHER |
| Jiangsu Wanbang Medicine Marketing Co., Ltd. | UNKNOWN |
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This study is designed to verify the clinical efficacy and safety of different statins in dyslipidemia patients, and explore the effects on glycometabolic in patients with impaired glucose regulation.
Study Objective:
Study Design: The study was an open-label, multi-center network register-based follow-up study.
The total sample size: 10000 participants.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Pitavastatin treatment | Experimental | The drug pitavastatin is given to the patient according to the doctor's order and restricted to BangZhi produced by Jiangsu Wanbang Medicine Marketing Co., Ltd.. |
|
| Atorvastatin treatment | Experimental | The drug atorvastatin is given to the patient according to the doctor's order and the drug band is unspecified. |
|
| Rosuvastatin treatment | Experimental | The drug atorvastatin is given to the patient according to the doctor's order and the drug band is unspecified. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Pitavastatin | Drug | Capsule/Tablet, oral, follow the doctor's advice Participants will receive pitavastatin treatment for 3 or 12 weeks. |
|
| Measure | Description | Time Frame |
|---|---|---|
| LDL-C target achieving rate | To measure the levels of LDL-C in mmol/L and calculate the LDL-C target achieving rate. | 3 months |
| Measure | Description | Time Frame |
|---|---|---|
| Blood lipid parameters | The levels of total cholesterol (TC) in mmol/L | 3 months |
| Blood lipid parameters | The levels of triglyceride (TG) in mmol/L |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Yuming Jin, Professor | School of Public Health,Fudan University | Principal Investigator |
| Dayi Hu, Professor | Director of Department of Cardiology, Peking University People's Hospital; Director of Institute of Cardiovascular Disease, Peking University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Heart Center of Peking University People's Hospital | Beijing | Beijing Municipality | 100044 | China | ||
| School of Public Health, Fudan University |
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| ID | Term |
|---|---|
| D050171 | Dyslipidemias |
| D002318 | Cardiovascular Diseases |
| D006973 | Hypertension |
| ID | Term |
|---|---|
| D052439 | Lipid Metabolism Disorders |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
| D014652 | Vascular Diseases |
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| ID | Term |
|---|---|
| C108475 | pitavastatin |
| D000069059 | Atorvastatin |
| D000068718 | Rosuvastatin Calcium |
| ID | Term |
|---|---|
| D011758 | Pyrroles |
| D001393 | Azoles |
| D006573 | Heterocyclic Compounds, 1-Ring |
| D006571 | Heterocyclic Compounds |
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Participants are assigned to one of two or more groups in parallel for the duration of the study.
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| Atorvastatin | Drug | Capsule/Tablet, oral, follow the doctor's advice Participants will receive atorvastatin treatment for 3 or 12 weeks. |
|
| Rosuvastatin | Drug | Capsule/Tablet, oral, follow the doctor's advice Participants will receive rosuvastatin treatment for 3 or 12 weeks. |
|
| 3 months |
| Blood lipid parameters | The levels of low density lipoprotein cholesterol (LDL-C) in mmol/L | 3 months |
| Blood glucose levels | To measure the level of glycosylated hemoglobin (HbA1) in percent (%) | 1 year |
| Fasting blood glucose | The levels of fasting blood glucose (FBG) in mmol/L | 1 year |
| Blood lipid parameters | The levels of total cholesterol (TC) in mmol/L | 1 year |
| Blood lipid parameters | The levels of triglyceride (TG) in mmol/L | 1 year |
| Blood lipid parameters | The levels of low density lipoprotein cholesterol (LDL-C) in mmol/L | 1 year |
| Blood lipid parameters | The levels of High density lipoprotein cholesterol (HDL-C) in mmol/L | 1 year |
| Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability] | To evaluate the safety and tolerability of the three statins, the incidence of treatment-emergent adverse events should be recorded though the study. | Through study completion, an average of 1 year |
| Shanghai |
| Shanghai Municipality |
| 200032 |
| China |
| D006538 |
| Heptanoic Acids |
| D005227 | Fatty Acids |
| D008055 | Lipids |
| D013449 | Sulfonamides |
| D000577 | Amides |
| D009930 | Organic Chemicals |
| D005464 | Fluorobenzenes |
| D006845 | Hydrocarbons, Fluorinated |
| D006846 | Hydrocarbons, Halogenated |
| D006838 | Hydrocarbons |
| D013450 | Sulfones |
| D013457 | Sulfur Compounds |
| D011743 | Pyrimidines |