- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT04956679
Family-based Screening and Treatment of Helicobacter Pylori:A Real World Study
11. oktober 2021 oppdatert av: Yanqing Li, Shandong University
The habit of family meals makes the infection rate of Helicobacter pylori high in China, which is also the main cause of reinfection of Helicobacter pylori.
Eating together can easily cause family members to be infected with Helicobacter pylori.
We used a real-world study to understand the risk factors, epidemiological characteristics, and safety and effectiveness of eradication therapy for helicobacter pylori infection in family-based screening and treatment.
Studieoversikt
Status
Rekruttering
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
Helicobacter pylori infection is a worldwide problem, which is the main cause of gastric cancer.
The habit of sharing meals in the family is one of the factors contributing to the high infection rate of HP in China, as well as the main cause of reinfection of HP.
Sharing meals can easily cause family members to be infected with HP.Family members live together, eat together, share tableware and other behaviors through the "mouth to mouth" transmission of Helicobacter pylori may be infected with each other, is also one of the reasons for the eradication of many patients after re-infection.At the same time, repeated infection and treatment of Helicobacter pylori will increase the difficulty of Helicobacter pylori reeradication.As a family unit, to study the status of our country family helicobacter pylori infection, epidemiological characteristics, infection risk factor, the different schemes, such as the safety and efficacy of treatment to take measures to reduce the infection rate is of great significance to prevention and treatment of gastric cancer.
Studietype
Observasjonsmessig
Registrering (Forventet)
400
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiekontakt
- Navn: Li Yanqing, PhD
- Telefonnummer: 053182169385
- E-post: liyanqing@sdu.edu.cn
Studer Kontakt Backup
- Navn: Li Yueyue, PhD
- Telefonnummer: 18560089751
- E-post: lyynqj@126.com
Studiesteder
-
-
Shandong
-
Jinan, Shandong, Kina, 250012
- Rekruttering
- Department of Gastroenterology,QiLu Hospital,Shandong University
-
-
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
3 år og eldre (Barn, Voksen, Eldre voksen)
Tar imot friske frivillige
Nei
Kjønn som er kvalifisert for studier
Alle
Prøvetakingsmetode
Sannsynlighetsprøve
Studiepopulasjon
Community population aged above 3 years in family unit,The family unit is determined by actual living together rather than household registration relationship, with at least 2 people in the family and living together for at least 10 months each year in the past 5 years.
Beskrivelse
Inclusion Criteria:
- Community population over 3 years old who signed the informed consent.
- at least 2 people in the family.
- living together for at least 10 months each year in the past 5 years except child aged below 5.
Exclusion Criteria:
- PPI drugs such as esomeprazole、pantoprazole、 rabeprazole,、lansoprazole、famotidine and H2 receptor antagonists were taken within two weeks.
- antibiotics、bismuth agents or traditional Chinese medicine with antibacterial effect were taken within four weeks
- There are other factors that researchers think are not suitable for participation
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Observasjonsmodeller: Familiebasert
- Tidsperspektiver: Potensielle
Kohorter og intervensjoner
Gruppe / Kohort |
Intervensjon / Behandling |
---|---|
Family members in the study
Community groups that meet the inclusion criteria
|
Patients with positive Helicobacter pylori infection were determined by carbon 13 breath test ,The diagnosis and treatment of positive patients were followed up without other intervention.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
---|---|---|
Patient compliance of performing medical examination.
Tidsramme: 1 year
|
Good compliance of medical examination advice was defined as the subjects took the medical advice given by the doctor and the rate of adoption and implementation of the medical examination advice.
|
1 year
|
Patient compliance of taking medication
Tidsramme: 1 year
|
Patient compliance of taking medication is defined as the ratio of the actual dose of medication taken by the patient to the total amount of medication required by the prescription.
Good medication compliance is defined as the ratio greater than 80%.
|
1 year
|
Number of participants with treatment-related adverse events as assessed by CTCAE v5.0
Tidsramme: 1 year
|
Adverse reactions related to medication were recorded
|
1 year
|
Lesion detection ratio
Tidsramme: 1 year
|
The lesion detection ratio was defined as the ratio of the number of subjects who underwent medical examination on the basis of doctor's recommendation and were finally diagnosed with lesion to the number of subjects who underwent examination.
|
1 year
|
Eradication rate
Tidsramme: 1 year
|
Eradication rate was defined as the ratio of the number of patients diagnosed positive on the carbon 13 breath test to the number of subjects who turned negative after taking the eradication drug to the number of subjects diagnosed positive before taking the drug.
|
1 year
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
---|---|---|
The high-risk factors of Helicobacter pylori infection in families were investigated by questionnaire statistics.
Tidsramme: 1 year
|
Questionnaire survey was used to conduct information statistics on families undergoing Helicobacter pylori screening.Statistics include family members of the general situation, basic information, personal health and life habit, individual disease history, personal nearly 1 month medications, family health and lifestyle, family history, history of HP infection and the eradication of history, screening results, doctor give opinions and patient adherence and follow-up outcome after screening process, etc. Statistical soft ware was used to analyze factor correlations.
|
1 year
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Etterforskere
- Studiestol: Li Yanqing, PhD, Qilu Hospital, Shandong University
Publikasjoner og nyttige lenker
Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Faktiske)
10. juli 2021
Primær fullføring (Forventet)
1. mai 2022
Studiet fullført (Forventet)
1. juni 2022
Datoer for studieregistrering
Først innsendt
25. juni 2021
Først innsendt som oppfylte QC-kriteriene
29. juni 2021
Først lagt ut (Faktiske)
9. juli 2021
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
12. oktober 2021
Siste oppdatering sendt inn som oppfylte QC-kriteriene
11. oktober 2021
Sist bekreftet
1. oktober 2021
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Andre studie-ID-numre
- 2019SDU-QILU-186
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Nei
Studerer et amerikansk FDA-regulert enhetsprodukt
Nei
produkt produsert i og eksportert fra USA
Nei
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .
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