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Study of Clinical Course of Newly Diagnosed Moderate to Severe Ulcerative Colitis in Korea

Cohort Study of Newly Diagnosed Moderate to Severe Ulcerative Colitis in Tertiary Referral Hospital Setting in Korea

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02229344
Acronym
MOSAIK
Enrollment
368
Registered
2014-09-01
Start date
2014-07-01
Completion date
2022-02-22
Last updated
2025-04-27

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

Conditions

Colitis, Ulcerative

Keywords

colitis, ulcerative, MOSAIK, REMICADE, Infliximab

Brief summary

The purpose of this study is to describe clinical course of newly diagnosed moderate to severe ulcerative colitis (chronic inflammatory disease of the colon) in tertiary referral hospitals in Korea for 5-year follow-up under usual care.

Detailed description

This is a multicenter (when medical research study takes place in more than one country), prospective (study following participants forward in time), disease-oriented and hospital-based 5-year follow-up longitudinal study in Korean participants with newly diagnosed moderate to severe ulcerative colitis who visit tertiary referral hospital. As the study is observational in nature, no intervention will be received by participants. Efficacy will primarily be assessed by number of relapses and percentage of participants achieving sustained remission (clinical, endoscopic and combined remission).

Interventions

OTHERNo Intervention

Participants with newly diagnosed moderate to severe ulcerative colitis in a tertiary referral hospital within 4 weeks before prior to enrollment will be observed.

Sponsors

Janssen Korea, Ltd., Korea
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
7 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Participant is newly diagnosed with moderate to severe ulcerative colitis in a tertiary referral hospital within 4 weeks prior to enrollment * The diagnosis was based on symptoms consistent with ulcerative colitis lasting for more than 4 weeks, excluding infections and other acute or chronic non-infectious bowel syndrome conditions * Participants meet diagnostic criteria for ulcerative colitisif at least 3 out of 4 of the following are met: 1) A History of diarrhea and/or blood/pus in stool, 2) Macroscopic appearance at endoscopy, with continuous mucosal inflammation affecting the rectum in continuity with some or all of the colon, 3) Microscopic features on biopsy consistent with ulcerative colitis, 4) No suspicion of Crohn's disease or indeterminate colitis * Participants are willing to participate in regular follow-up visits * Participant is willing to participate in the study and has signed the informed consent

Exclusion criteria

* Participants in an interventional clinical trial with systemic corticosteroid, biologics (including, but not limited to, infliximab, golimumab, adalimumab and vedolizumab, etc) and other drugs (sulfasalazine, medalamine, azathioprine, tofacitinib, etc) for ulcerative colitis * Having experienced colectomy such as subtotal colectomy with ileorectostomy or colectomy with ileoanal pouch, Koch pouch, or ileostomy for ulcerative colitis, or planning surgical treatment within 1 year from enrollment * A current diagnosis of indeterminate colitis, or current diagnosis or history of Crohn's disease

Design outcomes

Primary

MeasureTime frameDescription
Total Number of Relapses in Year 1Year 1Relapse is defined as increase in Mayo or partial Mayo score of more than or equal to (\>=) 3 points from clinical response or remission. Mayo score is a discrete ordinal scale with total score ranging from 0 (normal or inactive disease) to 12 (severe disease) and partial Mayo score ranges from 0 (normal or inactive disease) to 9 (severe disease). Relapses will be categorized as: infrequent (less than or equal to \[\<=\] 1 relapse per year), frequent pattern (\>=2 relapses per year) and continuous (persistent symptoms of active ulcerative colitis without a period of remission).
Total Number of Relapses in Year 3Year 3Relapse is defined as increase in Mayo or partial Mayo score of \>=3 points from clinical response or remission. Mayo score is a discrete ordinal scale with total score ranging from 0 (normal or inactive disease) to 12 (severe disease) and partial Mayo score ranges from 0 (normal or inactive disease) to 9 (severe disease). Relapses will be categorized as: infrequent (\<=1 relapse per year), frequent pattern (\>=2 relapses per year) and continuous (persistent symptoms of active ulcerative colitis without a period of remission).
Total Number of Relapses in Year 5Year 5Relapse is defined as increase in Mayo or partial Mayo score of \>=3 points from clinical response or remission. Mayo score is a discrete ordinal scale with total score ranging from 0 (normal or inactive disease) to 12 (severe disease) and partial Mayo score ranges from 0 (normal or inactive disease) to 9 (severe disease). Relapses will be categorized as: infrequent (\<=1 relapse per year), frequent pattern (\>=2 relapses per year) and continuous (persistent symptoms of active ulcerative colitis without a period of remission).
Percentage of Participants With Sustained Remission in Year 1Year 1Clinical remission is \<=2 points with no individual sub-score \>1 point using total or partial Mayo Score. Mayo score is a discrete ordinal scale with total score ranging from 0 (normal or inactive disease) to 12 (severe disease) and partial Mayo Score score ranges from 0 (normal or inactive disease) to 9 (severe disease).
Percentage of Participants With Sustained Remission in Year 3Year 3Clinical remission is \<=2 points with no individual sub-score \>1 point using total or partial Mayo Score. Mayo score is a discrete ordinal scale with total score ranging from 0 (normal or inactive disease) to 12 (severe disease) and partial Mayo Score score ranges from 0 (normal or inactive disease) to 9 (severe disease).
Percentage of Participants With Sustained Remission in Year 5Year 5Clinical remission is \<=2 points with no individual sub-score \>1 point using total or partial Mayo Score. Mayo score is a discrete ordinal scale with total score ranging from 0 (normal or inactive disease) to 12 (severe disease) and partial Mayo Score score ranges from 0 (normal or inactive disease) to 9 (severe disease).

Secondary

MeasureTime frameDescription
Mean Change From Baseline in Disease Extent at Year 1, 3 and 5Baseline, Year 1, 3 and 5Colonoscopy (a medical examination of the colon by a physician using a colonoscope) will be conducted to explore the extent of lesion to determine extent of disease.
Mean Change From Baseline in Inflammatory Bowel Disease Questionnaire (IBDQ) Score at Year 1, 3 and 5Baseline and Year 1, 3 and 5The IBDQ evaluates the effect of the participants' inflammatory bowel disease on the quality of life Scores range from 32 to 224 with higher scores indicating better quality of life.
Mean Change From Baseline in Short Form Survey (SF 12) Score at Year 1, 3 and 5Baseline, Year 1, 3 and 5The SF12 is a generic measure physical and mental health, it is is weighted and summed to provide easily interpretable scales. Physical and Mental Health Composite Scores (PCS & MCS) are computed using the scores of twelve questions and range from 0 to 100, where a zero score indicates the lowest level of health measured by the scales and 100 indicates the highest level of health.
Mean Time to RelapseYear 1, 3 and 5Relapse is defined as increase in mayo or partial Mayo score of more than or equal to (\>=) 3 points from clinical response or remission. Mayo score is a discrete ordinal scale with total score ranging from 0 (normal or inactive disease) to 12 (severe disease) and partial Mayo score ranges from 0 (normal or inactive disease) to 9 (severe disease). Average time taken to occurrence of first relapse will be observed.
Percentage of Participants Treated With Immune Modulators, Systemic Steroids and BiologicsBaseline up to Year 5Percentage of participants treated with immune modulators (azathioprine or 6-mercaptoprine at least a consecutive 3-month course), systemic steroids and biologics will be reported.
Mean Time to First Treatment With Immune Modulators, Systemic Steroids and Biologics From BaselineBaseline up to Year 5Time to first administration of immune modulators like azathioprine or 6-mercaptoprine for at least a consecutive 3-month course, systemic steroids and biologics from Baseline will be observed.
Number of Participants With Complementary and Alternative Medicine (CAM) use and SatisfactionBaeline up to Year 5Number of participants with CAM use and satisfaction will be reported.
Change From Baseline in Hospital Anxiety and Depression Scale (HADS) Score at Year 1, 3 and 5Baseline, Year 1, 3 and 5The HADS is a self-assessment scale for the symptom severity of anxiety disorders and depression. It comprises of 14 items, and each item is rated on a four-point scale (0-3). All seven answers are summarized and calculated to a total score to the anxiety scale and to the depression scale with a maximum score of 21 points for each scale.
Percentage of Participants With Sustained Clinical ResponseYear 1, 3 and 5Response is defined as decrease in Mayo or partial Mayo score of \>=3 points from Baseline and decrease in Mayo score of \>=30 percent (%) from Baseline and decrease in the rectal bleeding score \>=1 or an absolute rectal bleeding score of 0 or 1.
Total Number of Ulcerative Colitis-Related HospitalizationsYear 3 and 5Total number of ulcerative colitis-related hospitalizations will be observed.
Total Days of Ulcerative Colitis-Related HospitalizationsYear 3 and 5Total days of ulcerative colitis-related hospitalizations will be observed.
Percentage of Participants With ColectomyYear 3 and 5Percentage of participants who will be going for surgery to remove part or all of the colon will be observed.
Percentage of Participants With DeathYear 3 and 5Percentage of participants with death (ulcerative colitis related and non-ulcerative colitis related) will be observed.

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026