- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02998944
The Study of CCTM and Common Diseases
16. december 2016 opdateret af: Zihui Tang, Shanghai Tongji Hospital, Tongji University School of Medicine
the Association Study of Constitution of Traditional Chinese Medicine and Common Diseases
This study aimed to explore the associations between constitutions of traditional Chinese medicine (TCM) and common disease (CD).
A large-scale, community-based, cross-sectional study was performed to investigate the associations.
A total of 3748 participants were available for analysis in this study.
The assessment of constitution of TCM was based on recommendations of Association Chinese Medicine in China.
In this study, the diagnosis of CD was based on self-reported medical history.
The associations were analyzed using univariate and multivariable logistic regression (MLR).
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
This study aimed to explore the associations between constitutions of traditional Chinese medicine (TCM) and common disease (CD).
A large-scale, community-based, cross-sectional study was performed to investigate the associations.
A total of 3748 participants were available for analysis in this study.
The assessment of constitution of TCM was based on recommendations of Association Chinese Medicine in China.
In this study, the diagnosis of CD was based on self-reported medical history.
The associations were analyzed using univariate and multivariable logistic regression (MLR).
Undersøgelsestype
Observationel
Tilmelding (Faktiske)
3748
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
30 år til 90 år (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Alle
Prøveudtagningsmetode
Sandsynlighedsprøve
Studiebefolkning
A risk-factor study for constitution of TCM and chronic disease was conducted in a random sample of the Chinese population.
Participants aged 30-90 years were recruited from rural and urban communities in Shanghai.
More than 4,000 participants were invited to a screening visit between 2011 and 2013.
Written consent was obtained from all patients before the study, which was performed in accordance with the ethical standards in the Declaration of Helsinki, and approved by the Medicine Ethical Committee of the Huashan Hospital.
The exclusion criteria were 1) severity renal and liver function abnormal and 2) pregnant woman.
A total of 3748 participants were available to data analysis.
Beskrivelse
Inclusion Criteria:
- Participants aged 30-90 years were recruited from rural and urban communities in Shanghai.
Exclusion Criteria:
- severity renal and liver function abnormal and pregnant woman
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
hypertension
Tidsramme: through study completion, an average of 2 year
|
questionaire
|
through study completion, an average of 2 year
|
diabetes mellitus
Tidsramme: through study completion, an average of 2 year
|
questionaire
|
through study completion, an average of 2 year
|
coronary artery disease
Tidsramme: through study completion, an average of 2 year
|
questionaire
|
through study completion, an average of 2 year
|
COPD
Tidsramme: through study completion, an average of 2 year
|
questionaire
|
through study completion, an average of 2 year
|
Obesty
Tidsramme: through study completion, an average of 2 year
|
calculation from height and weight
|
through study completion, an average of 2 year
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Samarbejdspartnere
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
Generelle publikationer
- Fang P, Dong J, Zeng F, Tang Z. Analysis of the association between glucose profiles and beta-cell function for diabetic cardiovascular autonomic neuropathy in China. J Diabetes Investig. 2017 May;8(3):354-362. doi: 10.1111/jdi.12584. Epub 2016 Nov 25.
- Lv Y, Zhou L, Tang Z, Dong J. Association and interaction analysis of diabetes mellitus and SCN10A for cardiovascular autonomic neuropathy in a Chinese population. Postgrad Med J. 2017 Jun;93(1100):344-348. doi: 10.1136/postgradmedj-2016-134202. Epub 2016 Oct 11.
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. januar 2011
Primær færdiggørelse (Faktiske)
1. december 2013
Studieafslutning (Faktiske)
1. november 2016
Datoer for studieregistrering
Først indsendt
4. december 2016
Først indsendt, der opfyldte QC-kriterier
16. december 2016
Først opslået (Skøn)
21. december 2016
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
21. december 2016
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
16. december 2016
Sidst verificeret
1. december 2016
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- cctmcd
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
INGEN
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
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