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Intervention of Food - Medicine Homology Formulas on Chronic Pharyngitis and Mechanism Study Based on Network Pharmacology

Intervention of Food - Medicine Homology Formulas on Chronic Pharyngitis and Mechanism Study Based on Network Pharmacology

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000639
Enrollment
Unknown
Registered
2026-03-20
Start date
2026-04-15
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Chronic Pharyngitis

Interventions

Experimental Group:tablet candy
Control Group:Platycodon grandiflorus (Jiegeng), Glycyrrhiza uralensis (Gancao),Ingredients

Sponsors

Qingdao University Qingdao Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Age range: 18 to 65 years old; (2) Meeting both Western medicine and traditional Chinese medicine diagnostic criteria for chronic pharyngitis; (3) Disease duration of = 3 months; (4) No relevant treatment or consumption of throat-clearing medications or foods within the past month; (5) Voluntary participation in this trial, with informed consent signed by the participant prior to the study.

Exclusion criteria

Exclusion criteria: (1) Patients in the acute exacerbation phase of other chronic diseases; (2) Patients with no obvious masses observed in the throat under electronic laryngoscopy, and further of other areas such as the nose, pharynx, larynx, trachea, esophagus, and neck for potential lesions causing symptoms; (3) High-risk populations, such as pregnant and breastfeeding women, and individuals with allergies to the test product; (4) Patients with severe primary diseases of the cardiovascular, liver, kidney, respiratory, circulatory, autoimmune, or hematopoietic systems, or patients with mental illness; (5) Patients who are uncooperative, have poor compliance, or have incomplete data; (6) Patients deemed by the investigator to have other factors making them unsuitable for inclusion.

Design outcomes

Primary

MeasureTime frame
TCM Syndrome Score;

Secondary

MeasureTime frame
blood sample;Oropharyngeal microbiome sample;Quality of Life Score for Chronic Pharyngitis;Laryngoscope;Urinalysis;Chest X-ray;Routine Electrocardiogram;

Countries

China

Contacts

Public ContactZhong Feng

Qingdao University

zhfoeg@163.com18661833099

Outcome results

None listed

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