Eligible participant has to fullfill all of the following items | / / / / |
Anyone with one of following items or more should be excluded: | / / / / / / / / |
- General information
- Medical history
- Physical examination
- Blood Routine Tests
- Urine Routine Test
- Blood Electrolytes Tests
- Coagulation Function Tests
- Serum Liver Function Tests
- HBV/HCV/HIV/Syphilis Markers Test
- Renel Function Test
- D-dimer
- hCG Test
- Image Examinations
- Visual Analogue Scale
- Blood Gas Analysis
Date of signing the informed consent |
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Date of birth | yyyy-mm-dd |
Age | Years |
Education background | |
Occupation | |
Other (Description) |
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小时 |
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|
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Number of pregnancy | 次 |
Number of delivery | 次 |
If has delivery history, select following items | |
partus maturus | 次 |
premature delivery | 次 |
abortion | 次 |
Last pregnancy | yyyy-mm-dd |
Average times of menstrual onset a year | 次/年 |
Average menstrual cycle | 天(days) |
Menarche time | 岁(years) |
The time of last Menstruation | 年、月、日(yyyy-mm-dd) |
The time of menstrual onset before the last one | 年、月、日(yyyy-mm-dd) |
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年/月/日(yyyy-mm-dd) |
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Namy of the drug to be allergied |
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Vulva | |
Description in detail for abnormal |
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Vagina | |
Description in detail for abnormal |
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Uterine neck | |
Description in detail for abnormal |
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Corpus uteri | |
Description in detail for abnormal |
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Adnexa uteri | |
Left side | |
Description in detail for abnormal |
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Right side | |
Description in detail for abnormal |
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Weight | kg |
Hight | mm |
Systolic pressure (SP) | mmHg |
Diastolic pressure | mmHg |
Temperature | degree Celsius |
Pulse rate | 次/分 |
Breath frequency | 次/分 |
Doctor signature |
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Date | yyyy-mm-dd |
WBC | ×109 /L |
NEUT% | % |
LY% | % |
MONO% | % |
RBC | ×10^12 /L |
HGB | g/L |
PLT | ×10^9 /L |
Researcher signature |
|
Date | yyyy-mm-dd |
Acidity and allkalinity | |
pH value |
|
Urine protein | |
Urine red cell | |
Urine WBC | |
Urine glucos | |
Urine Bilirubin | |
Urine HCG | |
KET | |
SG |
|
UBG | |
NIT | |
Date of test | yyyy-mm-dd |
Date of test | yyyy-mm-dd |
K | mmol/L |
Na | mmol/L |
Cl | mmol/L |
Ca | mmol/L |
P | mmol/L |
Date of examination | yyyy-mm-dd |
Prothrombin time | 秒 |
Thrombin time (TT) | 秒 |
Activated partial thromboplastin time (APTT) | 秒 |
Fibrinogen (FIB) | g/L |
ALT | IU/L |
AST | 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 |
Date of test | yyyy-mm-dd |
Date of test | yyyy-mm-dd |
Date of test | yyyy-mm-dd |
Date of test | yyyy-mm-dd |
Date of test | yyyy-mm-dd |
SCr | μmol/L |
Blood urea | mmol/L |
Blood uric acid | μmol/L |
Date of test | yyyy-mm-dd |
D-dimer value | ug/mL |
Date of test |
|
Urine pregnancy test | |
Blood HCG concentration | mIU/mL |
Date of test | yyyy-mm-dd |
Size of the ulcer | cm*cm |
Uterine echo distribution | |
Endometrial thickness | mm |
Left ovary size | cm ×cm |
Shape of Left ovary | |
Size of the Ovarian cyst |
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Right ovary size | cm ×cm |
Shape of right ovary | |
Size of Ovarian cyst |
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Description of other abnormal findings |
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Diagnosis of the Ultrasound B |
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Doctor signature |
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Date of examination | yyyy-mm-dd |
Pain Visual Analogue Score |
PH |
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PCO2 | mmHg |
P02 | mmHg |
SO2 | % |
HCO3 | mmol/l |
SBE | mmol/l |
LAC | mmol/L |
Date of examination | (yyyy-mm-dd) |
右卵巢 |
|
3 cm |
|
无 ° |
|
/ | |
刘义彬 |
|
2024-1-26 |
D-dimer value | 0.35 ug/mL |
Date of test | 2024-1-27 |
Body temperature | 36.4 ℃ |
Systolic pressure (SP) | 135 mmHg |
Diastolic pressure (DP) | 84 mmHg |
Heart Rate, HR | 84 次/分 |
Pulse | 36.4 次/秒 |
WBC | 10.00 ×109 /L |
NEUT% | 77.82 % |
LY% | 16.18 % |
MONO% | 5.47 % |
RBC | 3.83 ×10^12 /L |
HGB | 104 g/L |
PLT | 288 ×10^9 /L |
Date | 2024-1-27 yyyy-mm-dd |
/ | |
Pain Visual Analogue Score | Occasionally very slight pain
|
sample collection | Collected
|
Volume | 2 ml |
Time of collection | 2024-1-27 yyyy-mm-dd-hh-min. |
Label Number of the sample | 2560436 |
Date received at DCC | -- yyyymmdd |
Report type | |
Name of this event | -- |
SAE start date | -- yyyymmdd |
SAE stop date | -- yyyymmdd |
Was this an unanticipated adverse event | |
Attribution to Study Drug | |
Outcome Type(check all that apply) | |
Recovery Description: (check only one) | |
Please provide a brief narrative of the SAE occurrence below | -- |
Name of the recorder | -- |
Data | -- yyyymmdd |
Site Investigator’s signature | -- |
Data | -- yyyymmdd |