Age
Item
1. patients whose age between 40 and 75 years old, male and female;
boolean
C0001779 (UMLS CUI [1])
Mild hypertension Stage | Systolic Pressure | Diastolic blood pressure
Item
2. patients who meet the diagnostic criteria of mild hypertension according to jnc-7 and china's prevention and cure guide of hypertension. mild hypertension (who/ish criteria stage i) systolic blood pressure 159≥(sbp) ≥140 and/or diastolic blood pressure 99≥(dbp) ≥90 .
boolean
C3276943 (UMLS CUI [1,1])
C1306673 (UMLS CUI [1,2])
C0871470 (UMLS CUI [2])
C0428883 (UMLS CUI [3])
Hypertension, mild | Antihypertensive Agents Absent
Item
3. patients who are initially diagnosed as mild hypertension or have been diagnosed as mild hypertension before but have not taken any antihypertensive drugs.
boolean
C3276943 (UMLS CUI [1])
C0003364 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Other Coding | Yin Deficiency | Yang Active Very | Obstruction Phlegm
Item
4. patients who are diagnosed as yue-yin style (yin-deficiency accompany with hyperactivity of yang) or yang-ming style (obstruction of phlegm and dampness) according to meridian syndrome differentiation
boolean
C3846158 (UMLS CUI [1])
C0085257 (UMLS CUI [2])
C2945617 (UMLS CUI [3,1])
C0205177 (UMLS CUI [3,2])
C0442824 (UMLS CUI [3,3])
C0028778 (UMLS CUI [4,1])
C0225378 (UMLS CUI [4,2])
Comprehension Study Protocol | Protocol Compliance
Item
5. patients who have a good understanding of our study. and willing to comply with our study protocol.
boolean
C0162340 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2])
Informed Consent | Informed Consent Relative
Item
6. informed consent form must be signed by patient or lineal relative.
boolean
C0021430 (UMLS CUI [1])
C0021430 (UMLS CUI [2,1])
C0080103 (UMLS CUI [2,2])
Criteria Fulfill
Item
7. all the tips are matched will be included.
boolean
C0243161 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
Secondary hypertension | Malignant Hypertension | Cushing Syndrome | Aortic coarctation | Pheochromocytoma | Renal parenchymal disease | Conn Syndrome | Hypertension, Renovascular | Sleep Apnea, Obstructive | Hypertensive disease Drug-induced
Item
1. patients who have been diagnosed as secondary hypertension or malignant hypertension(e.g. cushing's syndrome, coarctation of the aorta,phaeochromocytoma, renal parenchymal disease,primary aldosteronism, renovascular hypertension, obstructive sleep apnoea,drug induced hypertension et al )
boolean
C0155616 (UMLS CUI [1])
C0020540 (UMLS CUI [2])
C0010481 (UMLS CUI [3])
C0003492 (UMLS CUI [4])
C0031511 (UMLS CUI [5])
C1841992 (UMLS CUI [6])
C1384514 (UMLS CUI [7])
C0020545 (UMLS CUI [8])
C0520679 (UMLS CUI [9])
C0020538 (UMLS CUI [10,1])
C0458082 (UMLS CUI [10,2])
Medical condition Severe | Endocrine System Diseases | Cardiovascular Diseases | Digestive System Disorders | Liver Dysfunction | Cerebrovascular Disorders | Kidney Diseases | Hematological Disease | Study Subject Participation Status Uncertain
Item
2. patients who accompany with other severe medical conditions (e.g. endocrine disorders, cardiovascular disease. digestive disease. hepatic dysfunction,cerebral vascular disease. renal disease. haematologic disease et al). who may be not safe to join our study.
boolean
C3843040 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0014130 (UMLS CUI [2])
C0007222 (UMLS CUI [3])
C0012242 (UMLS CUI [4])
C0086565 (UMLS CUI [5])
C0007820 (UMLS CUI [6])
C0022658 (UMLS CUI [7])
C0018939 (UMLS CUI [8])
C2348568 (UMLS CUI [9,1])
C0087130 (UMLS CUI [9,2])
Chronic disease Inappropriate Clinical Trial | Epilepsy
Item
3. patients with a chronic disease which might not suitable for our study. e.g: epilepsy
boolean
C0008679 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0014544 (UMLS CUI [2])
Severe depression | Anxiety Severe | Zung's self-rating anxiety scale | Zung self-rating depression scale | Psychotic Disorder | Patient constitution allergic | Communicable Diseases
Item
,severe depression or anxiety (sas≥70,sds≥70) ,psychosis, allergic constitution, accompany with any infection.
boolean
C0588008 (UMLS CUI [1])
C0003467 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0451595 (UMLS CUI [3])
C0451593 (UMLS CUI [4])
C0033975 (UMLS CUI [5])
C0683521 (UMLS CUI [6,1])
C0700624 (UMLS CUI [6,2])
C0009450 (UMLS CUI [7])
Pregnancy | Breast Feeding | Pregnancy, Planned
Item
4. pregnant women or women in lactation or women of child bearing potential plan to conceive in the recent six months.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
Study Subject Participation Status
Item
5. patients who currently participate in another clinical trial.
boolean
C2348568 (UMLS CUI [1])
Acupuncture Recent
Item
6. patients who had been treated with acupuncture during the previous three months
boolean
C0394664 (UMLS CUI [1,1])
C0332185 (UMLS CUI [1,2])
Criteria Fulfill
Item
7. if one of the tips mentioned above is matched will be excluded.
boolean
C0243161 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])