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Analysis of the Impact of Helicobacter Pylori on Salivary Microbiome in Adults

Analysis of the Impact of Helicobacter Pylori Infection and Eradication on Salivary Microbiome in Adults by 16S Pyrosequencing

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03730766
Enrollment
60
Registered
2018-11-05
Start date
2018-08-01
Completion date
2018-11-20
Last updated
2018-11-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Helicobacter Pylori Infection

Keywords

helicobacter pylori, saliva microbiota

Brief summary

Helicobacter pylori (H. pylori), a bacteria transmitted from human to human through upper digestive tract as well as fecal-oral transmission, had infected more than half of people around the world. However, the quantity of H. pylori in oral cavity and its influence on oral microbiota remains to be unclear. The aim of the present study was to examine the effects of H. pylori infection as well as its eradication on oral microbiota.

Interventions

DRUGEsomeprazole

Proton pump inhibitor

DRUGAmoxicillin

Antibiotics for H. pylori eradication

DRUGBismuth Potassium Citrate

Gastric mucosal protective drug with anti-H. pylori effect

Sponsors

Shanghai Jiao Tong University School of Medicine
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Participants with non-ulcer functional dyspepsia or peptic ulcer disease * Ability and willingness to participate in the study and to sign and give informed consent * Received both endoscopy and 13C urea breath test (13C-UBT) before enrolled

Exclusion criteria

* Less than 18 years old * With previous gastric surgery * Major systemic diseases * Pregnancy or lactation * Allergy to any of the study drugs Administration of antibiotics, bismuth, antisecretory drugs in 8 weeks prior to inclusion * The use of antibiotics or PPI within 2 months before the study * The presence of dental carious or any untreated cavitated carious lesions and oral abscesses

Design outcomes

Primary

MeasureTime frameDescription
Change of saliva microbiota after eradicationTwo months after completion of therapy.Two months after completion of therapy, saliva microbiota was assessed by 16S rDNA Pyrosequencing.

Countries

China

Contacts

Primary ContactYingjie Ji, M.D.
jiyingjie39@outlook.com86+15800575527

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026