INSURE: A Cohort Study Comparing IFX to CS for Moderate to Severe UC

Sponsor
Sixth Affiliated Hospital, Sun Yat-sen University (Other)
Overall Status
Recruiting
CT.gov ID
NCT04879966
Collaborator
(none)
342
1
31.5
10.9

Study Details

Study Description

Brief Summary

The first-line treatment strategy of moderate to severe UC was a important question at issue. The biological agents had potentiality to alter the disease course of UC. The AGA clinical guidelines had conditional recommend that IFX and other biological agene migtht be first-line therapy for high-risk UC patints but only had low grade evidence.We launched this multicenter prospective cohort trial to compare the efficacy and safety of infliximab (IFX) and corticosteroids(CS) when they was used as first-line therapy in UC patients.

Condition or Disease Intervention/Treatment Phase

Study Design

Study Type:
Observational
Anticipated Enrollment :
342 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
A Multicenter Prospective Cohort Study Comparing Infliximab to Corticosteroids for Moderate to Severe Ulcerative Colitis
Anticipated Study Start Date :
May 17, 2021
Anticipated Primary Completion Date :
Dec 31, 2022
Anticipated Study Completion Date :
Dec 31, 2023

Arms and Interventions

Arm Intervention/Treatment
UC cohort

the patiente of Moderate to Severe Ulcerative Colitis who recieved infliximab(IFX) or corticosteroids(CS) as induction therapy would be enrolled in this cohort

Drug: Infliximab
Infliximab was used as induction therapy in UC patients, the maintenance treatment was decided by the researcher
Other Names:
  • IFX
  • Drug: Corticosteroid
    Corticosteroids was used as induction therapy in UC patients, the maintenance treatment was decided by the researcher
    Other Names:
  • CS
  • Outcome Measures

    Primary Outcome Measures

    1. clinical remission [week 14]

      defined as a total score of ≤2 on the Mayo scale and no subscore >1 on any of the four components

    Secondary Outcome Measures

    1. clinical response in induction phase [week 14]

      defined as a reduction in the partial Mayo score [stool frequency, rectal bleeding, and physician's global assessment] of ≥2 points and of ≥25% from baseline, with an accompanying decrease in rectal bleeding subscore of ≥1 point or absolute rectal bleeding subscore of ≤1 point

    2. mucosal healing in induction phase [week 14]

      defined as a subscore of 0 or 1 on the Mayo endoscopic component

    3. histological healing in induction phase [week 14]

      defined as Nancy index score of 0

    4. clinical response in maintenance phase [week 52]

      defined as a reduction in the partial Mayo score [stool frequency, rectal bleeding, and physician's global assessment] of ≥2 points and of ≥25% from baseline, with an accompanying decrease in rectal bleeding subscore of ≥1 point or absolute rectal bleeding subscore of ≤1 point

    5. mucosal healing in maintenance phase [week 52]

      defined as a subscore of 0 or 1 on the Mayo endoscopic component

    6. histological healing in maintenance phase [week 52]

      defined as Nancy index score of 0

    7. quality of life in induction phase [week 14]

      defined as an increase of ≥16 points in IBDQ score

    8. quality of life in maintenance phase [week 52]

      defined as an increase of ≥16 points in IBDQ score

    9. adverse events [week 52]

      as assessed by the incidence of adverse events

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 70 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • moderately to severely active ulcerative colitis, defined as a total score of 6 to 12 on the Mayo scale (scores range from 0 to 12, with higher scores indicating more severe disease) and a subscore of at least 2 on the endoscopic component of the Mayo scale (subscores on each of the four components of the Mayo scale range from 0 to 3)

    • Patients who had colonic involvement of at least 15 cm

    • Patients who had a confirmed diagnosis of ulcerative colitis at least 3 months before screening and confirmed by Pathology

    Exclusion Criteria:
    • Patients who had previously used any TNF inhibitor

    • Patients who were steroid-dependent or steriod-resistant

    • Patients who had undergone subtotal colectomy or total colectomy

    • Patients who had stoma

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 The Sixth Affiliated Hospital, Sun Yat-sen University Guandong China

    Sponsors and Collaborators

    • Sixth Affiliated Hospital, Sun Yat-sen University

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Sixth Affiliated Hospital, Sun Yat-sen University
    ClinicalTrials.gov Identifier:
    NCT04879966
    Other Study ID Numbers:
    • 2021ZSLYEC-102
    First Posted:
    May 10, 2021
    Last Update Posted:
    May 27, 2021
    Last Verified:
    May 1, 2021
    Studies a U.S. FDA-regulated Drug Product:
    Yes
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 27, 2021