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Clinical Study on Qingyou Mouthwash Combined with Quadruple Therapy for Helicobacter pylori-Related Halitosis

Clinical Study on Qingyou Mouthwash Combined with Quadruple Therapy for Helicobacter pylori(Hp)-Related Halitosis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000889
Enrollment
Unknown
Registered
2024-12-29
Start date
2025-01-01
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Helicobacter pylori-Related Halitosis

Interventions

control group:Take Esomeprazole Enteric-coated Capsules (20mg bid) Amoxicillin Capsules (500mg bid) Clarithromycin Tablets (500mg bid) and Colloidal Bismuth Pectin Capsules (200mg bid) orally. Stop af
treatment group:Use "Qingyou Mouthwash" to rinse the mouth on the basis of the "Quadruple Therapy". It will be decocted uniformly on behalf of patients by Yixing Hospital of Traditional Chinese Medici

Sponsors

Yixing Traditional Chinese Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Meet the diagnostic criteria for Helicobacter pylori (Hp) infection; 2.Meet the diagnostic criteria for halitosis; 3.Meet the traditional Chinese medicine diagnostic criteria for the syndrome of dampness-heat in the spleen and stomach. 4.Have not previously received Hp eradication treatment; 5.Be aged between 18 and 65 with no gender restrictions; 6.Provide informed consent and voluntarily accept treatment.

Exclusion criteria

Exclusion criteria: 1.Patients who have used proton pump inhibitors (PPIs) within 2 weeks or antibiotics bismuth agents or other medications within 4 weeks; 2.Patients with oral diseases such as dental caries periodontitis or other oral diseases causing halitosis; 3.Patients with halitosis caused by upper respiratory tract infections with oral infections infections due to liver and biliary or urinary system diseases or halitosis due to poor lifestyle habits such as smoking and alcohol consumption; 4.Patients with allergic constitutions or known allergies to the drug components involved in this observation; 5.Patients with peptic ulcers gastric cancer or those who have undergone gastrointestinal surgery; 6.Patients with severe cardiopulmonary hepatic renal diseases and patients with mental illnesses; 7.Pregnant or breastfeeding women. Patients who meet any of the above criteria are not eligible to participate in this clinical observation.

Design outcomes

Primary

MeasureTime frame
Clinical efficacy evaluation of halitosis;

Secondary

MeasureTime frame
Changes in the Halitosis-related Quality of Life Test (HALT);Evaluation of the efficacy of Helicobacter pylori eradication;Changes in traditional Chinese medicine syndrome scores.;

Countries

China

Contacts

Public ContactRuyi Ji

Yixing Traditional Chinese Medicine Hospital

642717416@qq.com15251827241

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026