- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT05295914
Performance of Novel Simplified Score for Chronic Hepatitis B Treatment Eligibility in Thailand
International and national guideline for chronic hepatitis B (HBV) infection treatment recommend initiated antiviral in high HBV viral loads patients with significant liver inflammation and significant liver fibrosis. In Thailand, HBV viral loads and liver elastography are limited available in seconds to tertiary care hospital.
Recently, many of simplified scoring system (TREAT-B score, WHO (World Health Organization)-simplified score and REACH-B score) were developed for assessment of antiviral initiation.
This study aim to evaluate the performance of simplified score for chronic HBV treatment compare to Thailand and international standard guideline.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
According to WHO Global health sector strategy on viral hepatitis 2016- 2021, WHO aim to global eliminate HBV infection within 2030. Main strategies for achievement are effective prevention and treatment.
International and national guideline for HBV infection treatment recommend initiated antiviral in high HBV viral loads patients with significant liver inflammation and significant liver fibrosis. Thus, HBV viral load and liver elastography are required for indication assessment. In low-to-middle income country such as Thailand, HBV viral loads and liver elastography are limited available in seconds to tertiary care hospital.
Recently, many of simplified scoring system (TREAT-B score, WHO-simplified score and REACH-B score) were developed for assessment of antiviral initiation.
This study aim to evaluate the performance of simplified score for chronic HBV treatment compare to Thailand and international standard guideline.
Undersøgelsestype
Tilmelding (Forventet)
Kontakter og lokationer
Studiekontakt
- Navn: Watcharasak Chotiyaputta, Assoc Prof
- Telefonnummer: 6624197281
- E-mail: watcharasak.cho@mahidol.ac.th
Undersøgelse Kontakt Backup
- Navn: Tawesak Tanwandee, Professor
- Telefonnummer: 6624197282
- E-mail: tawesak@gmail.com
Studiesteder
-
-
-
Bangkok, Thailand, 10700
- Siriraj Hospital
-
Kontakt:
- Watcharasak Chotiyaputta, Asso Prof
- Telefonnummer: 6624197281
- E-mail: watcharasak.cho@mahidol.ac.th
-
Kontakt:
- Tawesak Tanwandee, Prof
- Telefonnummer: 6624197282
- E-mail: tawesak@gmail.com
-
Ledende efterforsker:
- Watcharasak Chotiyaputta, Asso Prof
-
Underforsker:
- Tawesak Tanwandee, Prof
-
Underforsker:
- Tanawat Geeratragool, MD
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Prøveudtagningsmetode
Studiebefolkning
Beskrivelse
Inclusion Criteria:
- Treatment naive chronic hepatitis B infection patients who visited at liver clinic and internal medicine clinic Siriraj hospital during January 2015-December 2021
- Age > 18 years
Exclusion Criteria:
- Treatment experience chronic hepatitis B infection patients
- HIV co-infection
- HCV (hepatitis C) co-infection
- concomitant HCC (hepatocellular carcinoma)
- Pregnancy
- Incomplete data
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
Intervention / Behandling |
|---|---|
|
Patient with chronic hepatitis B infection
Patient with chronic hepatitis B infection visited at liver and internal medicine clinic, Siriraj hospital between January 2015-2020
|
TREAT-B score: ALT(alanine transferase), HBeAg REACH-B score: sex, ALT, HBV viral load, age WHO-simplified score: ALT, cirrhosis
Andre navne:
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Performance of TREAT-B score for eligible antiviral treatment
Tidsramme: at 1st OPD(out patient department) visit through initiation of antivirus or 1 year (if not indication for antivirus)
|
Gold standard: Eligible antiviral treatment according to EASL (European Association for the Study of the Liver) criteria Description: performance was define by sensitivity(%), specificity(%), PPV(positive predictive value)(%), NPV (negative predictive value)(%), positive LR(likelihood ratio), negative LR
|
at 1st OPD(out patient department) visit through initiation of antivirus or 1 year (if not indication for antivirus)
|
|
Performance of WHO simplified score for eligible antiviral treatment
Tidsramme: at 1st OPD visit through initiation of antivirus or 1 year (if not indication for antivirus)
|
Gold standard: Eligible antiviral treatment according to EASL criteria Description: performance was define by sensitivity(%), specificity(%), PPV(%), NPV(%), positive LR, negative LR
|
at 1st OPD visit through initiation of antivirus or 1 year (if not indication for antivirus)
|
|
Performance of REACH-B score for eligible antiviral treatment
Tidsramme: at 1st OPD visit through initiation of antivirus or 1 year (if not indication for antivirus)
|
Gold standard: Eligible antiviral treatment according to EASL criteria Description: performance was define by sensitivity(%), specificity(%), PPV(%), NPV(%), positive LR, negative LR
|
at 1st OPD visit through initiation of antivirus or 1 year (if not indication for antivirus)
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Performance of TREAT-B score for eligible antiviral treatment
Tidsramme: at 1st OPD visit through initiation of antivirus or 1 year (if not indication for antivirus)
|
Gold standard: Eligible antiviral treatment according to Thai guideline criteria Description: performance was define by sensitivity(%), specificity(%), PPV(%), NPV(%), positive LR, negative LR
|
at 1st OPD visit through initiation of antivirus or 1 year (if not indication for antivirus)
|
|
Performance of WHO simplified score for eligible antiviral treatment
Tidsramme: at 1st OPD visit through initiation of antivirus or 1 year (if not indication for antivirus)
|
Gold standard: Eligible antiviral treatment according to Thai guideline criteria Description: performance was define by sensitivity(%), specificity(%), PPV(%), NPV(%), positive LR, negative LR
|
at 1st OPD visit through initiation of antivirus or 1 year (if not indication for antivirus)
|
|
Performance of REACH-B score for eligible antiviral treatment
Tidsramme: at 1st OPD visit through initiation of antivirus or 1 year (if not indication for antivirus)
|
Gold standard: Eligible antiviral treatment according to Thai guideline criteria Description: performance was define by sensitivity(%), specificity(%), PPV(%), NPV(%), positive LR, negative LR
|
at 1st OPD visit through initiation of antivirus or 1 year (if not indication for antivirus)
|
Samarbejdspartnere og efterforskere
Sponsor
Efterforskere
- Ledende efterforsker: Watcharasak Chotiyaputta, Assoc prof, Mahidol University
Datoer for undersøgelser
Studer store datoer
Studiestart (Forventet)
Primær færdiggørelse (Forventet)
Studieafslutning (Forventet)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
- Sygdomme i fordøjelsessystemet
- RNA-virusinfektioner
- Virussygdomme
- Infektioner
- Blodbårne infektioner
- Overførbare sygdomme
- Leversygdomme
- Hepatitis, viral, menneskelig
- Hepadnaviridae infektioner
- DNA-virusinfektioner
- Enterovirus infektioner
- Picornaviridae infektioner
- Hepatitis B
- Hepatitis
- Hepatitis A
- Hepatitis B, kronisk
- Hepatitis, kronisk
Andre undersøgelses-id-numre
- Si 745/2021
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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 .