- Screening
- Baseline
- In the process of the treatment
- At the end of the treatment
- Follow-up 1
- Follow-up 2
- Follow-up 3
- Management system of participants
- Speciman management system
- Data management system
- ADR/ADE management system
- Madicine management system
- Instruments management system
- SOPs
- Research team
- Design, Methods
Eligible participant has to fullfill all of the following items | / / / / / / |
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Date | yyyy-mm-dd |
- General information
- Physical examination
- Blood Routine Tests
- Urine and Stool Routine Tests
- Glucose test
- Serum Liver Function Tests
- Renel Function Test
- Heat Function Examination
- Image Examinations
Gender | Male
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Your age | 72 岁(years) |
Date of birth: | 1947 yyyy-mm-dd |
Nationality | Han
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Marriage history | |
Pulse rate | 次/分 |
Breath frequency | 次/分 |
Systolic pressure (SP) | mmHg |
Diastolic pressure | mmHg |
Did you experienced any drug allergy? | |
Namy of the drug to be allergied |
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Date of drug allergy happened | yyyy-mm-dd/mm-dd |
Doctor signature |
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Date | yyyy-mm-dd |
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Wagner grade | |
Signature of the doctor |
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Date of examination | yyyy-mm-dd |
WBC | 11 ×109 /L |
NEUT% | 70.4 % |
LY% | 18.4 % |
MONO% | 6.5 % |
RBC | 5.51 ×10^12 /L |
HGB | 148 g/L |
PLT | 270 ×10^9 /L |
Date | yyyy-mm-dd |
Acidity and allkalinity | Acidity
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pH value | 5.5 |
Urine protein | Suspending
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Urine red cell | Negative
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Urine WBC | Negative
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Urine glucos | Positive+++
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Urine Bilirubin | Negative
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Urine HCG | Negative
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KET | Negative
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SG | 1.02 |
UBG | Negative
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NIT | Negative
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Date of test | yyyy-mm-dd |
Fasting blood glucos concentration | 17.2 mmol/L |
Two hours after breakfast | mmol/L |
Two hours after lunch | mmol/L |
Two hours after dinner | mmol/L |
Date of test | yyyy-mm-dd |
CRP | mg/L |
Date of test | yyyy-mm-dd |
Fib | g/L |
t-PA | ug/L |
PAI-1 | ug/L |
Date of test |
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HbA1c | % |
Date of test | yyyy-mm-dd |
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Signature of the doctor |
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Date of examination | yyyy-mm-dd |
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ALT | 45 IU/L |
AST | 23 IU/L |
γ-Glutamyltransferase | 124 IU/L |
Serum bilirubin | 8.1 μmol/L |
Indirect bilirubin | 4.7 umol/L |
Direct bilirubin | 3.4 umol/L |
Serum albumin | 31 g/L |
Serum total protein | 74 g/L |
Date of test | yyyy-mm-dd |
Blood uric acid | 264 μmol/L |
SCr | 69 μmol/L |
Blood urea | 3.9 mmol/L |
Date of test | yyyy-mm-dd |
Ultrasonic echocardiography, UCG | |
Description in detail for abnormal |
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Date of examination | yyyy-mm-dd |
AST | U |
LDH | IU |
Lactic dehydrogenase isoenzyme | |
α-HBDH | U/L |
Creatine Kinase, CK | U/L |
Creatine kinase isoenzyme, CKMB | U/L |
Date of tests | yyyy-mm-dd |
/uploads/patrecord/5541/param337311/b0d906d9-8593-4e7a-9b06-712f65e989b8.jpg |
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Signature of the doctor |
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yyyy-mm-dd |
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ALT | IU/L |
AST | IU/L |
AST/ALT |
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γ-Glutamyltransferase | IU/L |
GGT | U/L |
Serum bilirubin | μmol/L |
Indirect bilirubin | umol/L |
Direct bilirubin | umol/L |
Serum albumin | g/L |
Serum globulin | g/L |
Serum total protein | g/L |
A/G |
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Date of test | yyyy-mm-dd |
BUN | 8mmol/L |
SCr | μmol/L |
Blood urea | mmol/L |
Blood uric acid | μmol/L |
Cr |
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Blood endogenous creatinine clearance | ml·s-1/m*2 |
BUN/Cr |
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Date of test | yyyy-mm-dd |
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ALT | IU/L |
AST | IU/L |
AST/ALT |
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γ-Glutamyltransferase | IU/L |
Serum bilirubin | μmol/L |
Indirect bilirubin | umol/L |
Direct bilirubin | umol/L |
Serum albumin | g/L |
Serum globulin | g/L |
Serum total protein | g/L |
A/G |
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Date of test | yyyy-mm-dd |
BUN | 8mmol/L |
SCr | μmol/L |
Blood urea | mmol/L |
Blood uric acid | μmol/L |
Cr |
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Date of test | yyyy-mm-dd |
- Management for Progress
- Blood Routine Tests
- Glucose test
- Liver Function Tests
- Renel Function Test
- Heat Function Examination
- Image Examinations
- Health Relative Quality of Life
Is there any additional combination drug? | |
次 |
WBC | ×109 /L |
NEUT% | % |
LY% | % |
MONO% | % |
RBC | ×10^12 /L |
HGB | g/L |
PLT | ×10^9 /L |
Researcher signature |
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Date | yyyy-mm-dd |
HbA1c | % |
Date of test | yyyy-mm-dd |
Blood glucose | mmol/L |
LAGE |
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MAGE |
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SDBG |
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MODD |
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LBGI |
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Date of test | yyyy-mm-dd |
Daily usage of insulin | IU |
Date of detection | yyyy-mm-dd |
ALT | IU/L |
AST | IU/L |
AST/ALT |
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γ-Glutamyltransferase | IU/L |
Serum bilirubin | μmol/L |
Indirect bilirubin | umol/L |
Direct bilirubin | umol/L |
Serum albumin | g/L |
Serum globulin | g/L |
Serum total protein | g/L |
A/G |
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Date of test | yyyy-mm-dd |
BUN | 8mmol/L |
SCr | μmol/L |
Blood urea | mmol/L |
Blood uric acid | μmol/L |
Cr |
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Date of test | yyyy-mm-dd |
Ultrasonic echocardiography, UCG | |
Description in detail for abnormal |
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Date of examination | yyyy-mm-dd |
AST | U |
LDH | IU |
Lactic dehydrogenase isoenzyme | |
α-HBDH | U/L |
Creatine Kinase, CK | U/L |
Creatine kinase isoenzyme, CKMB | U/L |
Date of tests | yyyy-mm-dd |
Before primary wounding | 分 |
Now (Current at moment) | 分 |
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Signature of the doctor |
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Date of examination | yyyy-mm-dd |
Whether got the informed consent? | |
Date of sign the informed consent | xx年xx月xx日 |
Adverse events | |
Name of the adverse event |
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Date of starting | yyyy-mm-dd |
Ending time | yyyy-mm-dd |
Does it continues to now | |
Severity | |
Corelation with the study drug | |
The method of treating the drug | |
The outcome | |
Is it sevious adverse event? | |
Did it resulted in stoped the study? | |
Possible reason of causing the adverse event | |
Person who report the adverse event |
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Time of the reporting | yyyy-mm-dd-hh-min. |