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Clinical study of endoscopic treatment for Patients with intestinal Behcet's disease having poor response to conventional treatment

Clinical study of endoscopic treatment for Patients with intestinal Behcet's disease having poor response to conventional treatment

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100044593
Enrollment
Unknown
Registered
2021-03-24
Start date
2021-03-15
Completion date
Unknown
Last updated
2021-09-20

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

Conditions

intestinal Behcet's disease

Interventions

Single group:Endoscopic injection of triamcinolone acetonide

Sponsors

The First Affiliated Hospital of Sun Yat-Sen University,
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 70 Years

Inclusion criteria

Inclusion criteria: Patients with Behcet's disease diagnosed in our hospital. The diagnostic criteria are in line with the diagnostic criteria for intestinal Behcet developed by the Korean IBD Cooperation Group in 2009. 1. Patients who have been ineffective after treatment with 5-aminosalicylic acid, corticosteroids, azathioprine or anti-tumor necrosis factor-a drugs for more than 8 weeks 2. Hormone dependent patients; 3. Number of ulcers <= 5.

Exclusion criteria

Exclusion criteria: 1. Patients suffering from other intestinal diseases such as Crohn's disease, intestinal tuberculosis, infectious enteritis, non-specific colitis, drug-related colitis, etc.; 2. Patients taking large amounts of immunosuppressive agents and glucocorticoids; 3. Patients with severe liver and kidney dysfunction; 4. Patients with contraindications to glucocorticoids, such as allergy to glucocorticoids, recent gastrointestinal anastomosis, diabetes, severe systemic infection, active peptic ulcer, history of severe mental illness, severe osteoporosis, high blood pressure Grade III, tuberculosis, etc.; 5. Patients with cardiovascular or cerebrovascular diseases using oral anticoagulants or antiplatelets.

Design outcomes

Primary

MeasureTime frame
8-week clinical remission rate and endoscopic mucosal healing rate;

Secondary

MeasureTime frame
52-week clinical remission rate and endoscopic mucosal healing rate;

Countries

China

Contacts

Public ContactHe Yao

The First Affiliated Hospital of Sun Yat-Sen University

heyaowyx@qq.com18928800393

Outcome results

None listed

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