Skip to content

Therapeutic Efficacy of Modified Mesalazine Enema in patients with Active Ulcerative Colitis

Therapeutic Efficacy of Modified Mesalazine Enema in Patients with Active Ulcerative Colitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500109779
Enrollment
Unknown
Registered
2025-09-25
Start date
2025-09-30
Completion date
Unknown
Last updated
2025-09-29

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

Conditions

Ulcerative colitis

Interventions

Experimental Group:For patients treated with mesalazine enema, a precise enema optimization system was adopted after routine guidance

Sponsors

Beijing Friendship Hospital ,Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Aged 18 years or older, meeting the diagnostic criteria for the active phase of ulcerative colitis as defined by the "Chinese Consensus on Diagnosis and Treatment of Inflammatory Bowel Disease (2018, Beijing)," with a disease duration of at least one month; 2.Currently undergoing mesalazine enema treatment; 3.Current mesalazine enema therapy.

Exclusion criteria

Exclusion criteria: 1.Patients unable to cooperate with the treatment; 2.Pregnant or breastfeeding patients; 3.Patients with severe underlying comorbidities, such as cardiovascular, cerebrovascular, hepatic, pulmonary, or renal diseases; 4.Patients with concurrent intestinal infections, intestinal obstruction, intestinal bleeding, or fulminant ulcerative colitis.

Design outcomes

Primary

MeasureTime frame
Enema retention time;Lichtiger Clinical Activity Index score;IBD Quality of Life Score;

Countries

China

Contacts

Public ContactSun Yue

Beijing Friendship Hospital ,Capital Medical University

386623849@qq.com+86 10 6313 8337

Outcome results

None listed

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