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Efficacy and Safety of Salecan in Chronic Disease patients

Efficacy and Safety of Salecan in Chronic Disease patients

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500112456
Enrollment
Unknown
Registered
2025-11-14
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Evaluate the regulatory effects of Salecan (ß-1,3/a-1,3 glucan) on blood glucose, blood lipids, blood pressure, obesity, visceral fat, uric acid, fatty liver, immune function, inflammation, oxidative stress, and intestinal flora, while investigating its efficacy in alleviating symptoms of chronic diseases such as rhinitis and inflammatory bowel disease (IBD).

Interventions

Control group:None
Intervention group:Oral Salecan

Sponsors

The First People's Hospital of Qinzhou
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Aged 18 to 75 years old (inclusive); 2.Able to understand and willing to strictly follow the research protocol to complete the trial, and has signed the informed consent form; 3.No congenital, neurological or psychiatric diseases (such as congenital heart disease, paralysis, deaf-mutism, dementia, mental disorders).

Exclusion criteria

Exclusion criteria: 1.Pregnant or lactating women; 2.Complicated with severe cardiac, hepatic or renal insufficiency, including but not limited to ALT and/or AST >= 2×ULN, serum creatinine >= 1.5×ULN, eGFR < 60 ml/(min×1.73m^2); 3.Complicated with severe organic diseases such as heart, liver, lung, brain diseases, or autoimmune diseases, malignant tumors; 4.Recent surgery, or receiving immunotherapy or other biological agents.

Design outcomes

Primary

MeasureTime frame
Twelve items of cytokines;Visceral fat;Immunoglobulin;Blood lipid;VAS;Erythrocyte sedimentation rate (ESR);Key indicators for blood glucose control;Inhalation and food allergen antibody determination IgE (20 tests);CRP;TNSS;Oxidative Stress;

Secondary

MeasureTime frame
TOSS;Gut microbiota;Rhinitis Control Assessment Test;Blood routine;Liver function;Renal function;Urinalysis;

Countries

China

Contacts

Public ContactYuanli Wang

The First People's Hospital of Qinzhou

wylxinyuan@126.com+86 777 281 9959

Outcome results

None listed

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