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Comparison of rectal with oral mesalazine in the treatment of Ulcerative Proctitis (CORRECT Study)

Comparison of rectal with oral mesalazine in the treatment of Ulcerative Proctitis (CORRECT Study) - CORRECT Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000010340
Enrollment
60
Registered
2013-04-01
Start date
2013-05-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Ulcerative colitis

Interventions

Randomized treatment with mesalazine suppository or oral mesalazine for 2 weeks Switch from oral mesalazine to mesalazine suppository for 2 weeks

Sponsors

Saitama Medical Center, Saitama Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients, more than 18 years old with active rectal type of ulcerative colitis 2. Patients treated with oral mesalazine drugs less than 2.4g for more than 2 weeks 3. Patients with active ulcerative colitis whose bloody stool scores are more than 1 4. Male or female, inpatients or outpatients will be permitted to be entered

Exclusion criteria

Exclusion criteria: 1. Patients started to be treated with rectal 5-ASA and/or rectal steroids within 30 days before entry 2. Patients started to be treated with oral steroids within 14 days before entry 3. Patients with pregnancy or with the possibility of pregnancy 4. Patients with allergy of mesalazine and/or salicylic acid 5. Patients who have experienced severe side effects of mesalazine. 6. Patients with liver and/or renal dysfunctuon 7. Patinets with malignancy or with the history of malignancy 8. Patients induced in remission with biologics or cyteapheresis 9. Patients diagnosed not to be appropriate in entry by doctors

Design outcomes

Primary

MeasureTime frame
Dissapearance rates of bloody stool on week 2

Countries

Japan

Contacts

Public ContactShingo Kato

Saitama Medical Center, Saitama Medical University Department of Gastroenterology and Hepatology

skato@saitama-med.ac.jp049-228-3564

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026