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Combination Corticosteroids+5-aminosalicylic Acids Compared to Corticosteroids Alone (for Ulcerative Colitis). (COMBOMESA)

Primary Purpose

Ulcerative Colitis

Status
Completed
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
5-ASA
Corticosteroids
Sponsored by
Centre Hospitalier Universitaire de Saint Etienne
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ulcerative Colitis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • UC known and diagnosed by established clinical-endoscopic and histological criteria or newly-diagnosed UC, based on clinical and endoscopic findings, and about to start treatment with corticosteroids.
  • Current hospitalization with Severe UC exacerbation as defined by a Lichtiger score of >10
  • Age >18
  • Has not been on oral systemic corticosteroids more than 14 days prior to hospitalization
  • If taking a thiopurine, the dose need to be stable for the last 2 months before admission

Exclusion Criteria:

  • Pregnant women
  • Allergy / unable to take prednisone / hydrocortisone/ 5-ASA.
  • Active infection - either enteric or elsewhere
  • Severe renal, liver or cardio respiratory comorbidity
  • Toxic megacolon, or clinical features suggestive of a need for imminent colectomy
  • Treatment with an anti-TNF within the prior 3 months
  • Prior treatment with cyclosporine or tacrolimus within the prior 3 months
  • Alcohol dependency
  • Unable or unwilling to provide informed consent
  • Participating in other clinical trial within the 2 months prior to admission

Sites / Locations

  • Chu Saint Etienne
  • Department of Gastroenterology Venizeleio General Hospital, Leoforos Knosou
  • Sheba Medical Center
  • Università di Roma Sapienza
  • Institute of Gastroenterology and Department of Internal Medicine, Yonsei University College of Medicine
  • Zvezdara University Clinical Center, Gastroenterology Department

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

5-ASA group

Control group

Arm Description

Patients will receive corticosteroids with optimized 5-ASA.

Patients will receive corticosteroids alone.

Outcomes

Primary Outcome Measures

Percentage of patients who respond to the treatment by day 7.
The primary endpoint will be the percentage of patients who respond to the treatment by day 7. Response will be defined by a drop of >3 points in the lichtiger score and an absolute score <10 on the two prior consecutive days without the need for rescue medications or surgery. In patients who improve and are discharged prior to day 7, the lichtiger score will be calculated based on the two last days of hospitalization, provided that at least 3 days of study medications were dispensed. Patients discharged before 3 days of study medications have been administered will be considered in-eligible and will be dropped out of the analyses.

Secondary Outcome Measures

Full Information

First Posted
January 25, 2016
Last Updated
August 25, 2021
Sponsor
Centre Hospitalier Universitaire de Saint Etienne
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1. Study Identification

Unique Protocol Identification Number
NCT02665845
Brief Title
Combination Corticosteroids+5-aminosalicylic Acids Compared to Corticosteroids Alone (for Ulcerative Colitis).
Acronym
COMBOMESA
Official Title
Combination Corticosteroids+5-aminosalicylic Acids Compared to Corticosteroids Alone in the Treatment of Moderate-severe Active Ulcerative Colitis: A Protocol of a Multi-center Prospective Randomized Investigator Blinded Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
August 2021
Overall Recruitment Status
Completed
Study Start Date
June 13, 2016 (Actual)
Primary Completion Date
May 11, 2021 (Actual)
Study Completion Date
May 11, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Universitaire de Saint Etienne

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The role of steroids in the treatment of severe ulcerative colitis (UC) exacerbation is well established and recommended by professional societies. Similarly, 5-aminosalycilates (5-ASA) agents in the form of mesalamine/mesalzine are well established proven therapy in mild-moderate UC, and the combination of oral 5-ASA with topical (per-rectal enema) 5-ASA was shown to be superior to oral 5ASA alone in patients with mild moderate UC. Thus, in most cases, when a patient with UC experiences a flare while taking 5-ASA therapy, treatment is usually optimized by maximizing the oral dose to 4gr/day and adding topical therapy until the flare is controlled. If this is unhelpful, or if the flare is severe to begin with, corticosteroids are usually prescribed. However, there are very scarce data comparing steroids versus 5-ASA in the treatment of severe UC exacerbation. The aim of this study is to compare the efficacy of steroids alone vs. combination of steroids + 5-ASA in the treatment of moderate-severe UC exacerbation.
Detailed Description
The role of steroids in the treatment of severe ulcerative colitis (UC) exacerbation is well established and recommended by professional societies. This recommendation is based on pivotal studies carried 50-60 years ago, by Truelove &Witts. Similarly, 5-aminosalycilates (5-ASA) agents in the form of mesalamine/mesalzine are well established proven therapy in mild-moderate UC, and the combination of oral 5-ASA with topical (per-rectal enema) 5-ASA was shown to be superior to oral 5ASA alone in patients with mild moderate UC. Thus, in most cases, when a patient with UC experiences a flare while taking 5-ASA therapy, treatment is usually optimized by maximizing the oral dose to 4gr/day and adding topical therapy until the flare is controlled. If this is unhelpful, or if the flare is severe to begin with, corticosteroids are usually prescribed. However, there are very scarce data comparing steroids versus 5-ASA in the treatment of severe UC exacerbation. In 1962 truelove et al compared topical and systemic corticosteroid therapy with sulphasalazine, and found steroids to be superior to sulfasalazine. Importantly, there are no data investigating whether the addition and/or continuation of 5-ASA agents as combination therapy with systemic corticosteroids is superior to corticosteroids alone in patients with moderate-severe active UC. This knowledge gap is pronounced in patients admitted to the hospital for intravenous corticosteroid treatment with moderate severe UC flare, in whom it is currently unknown if the addition of 5-ASA (Oral and/or topical) to corticosteroids will confer additional benefit and improve patients outcomes. Thus, in practical terms, the decision whether to stop or continue 5-ASA treatment or whether to add 5-ASA to steroids in the treatment of moderate-severe UC exacerbation is taken on an arbitrary basis. This is important shortcoming and knowledge gap in current medicine, as patients admitted with moderate-severe UC flare who do not respond to corticosteroids and require salvage therapy with infliximab, cyclosporine, or even urgent colectomy. This makes it prudent to explore any avenue for possible improvement of response to corticosteroids in this setting, for instance by addition of 5ASA. The aim of this study is: To compare the efficacy of steroids alone vs. combination of steroids + 5-ASA in the treatment of moderate- severe UC exacerbation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ulcerative Colitis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
160 (Actual)

8. Arms, Groups, and Interventions

Arm Title
5-ASA group
Arm Type
Experimental
Arm Description
Patients will receive corticosteroids with optimized 5-ASA.
Arm Title
Control group
Arm Type
Active Comparator
Arm Description
Patients will receive corticosteroids alone.
Intervention Type
Drug
Intervention Name(s)
5-ASA
Other Intervention Name(s)
5-aminosalicylates
Intervention Description
5ASA treatment (oral 5ASA will be given to all patients in this arm, in addition to topical 5ASA in patients who tolerate it).
Intervention Type
Drug
Intervention Name(s)
Corticosteroids
Other Intervention Name(s)
Usual care
Intervention Description
Corticosteroids will be given to all patients.
Primary Outcome Measure Information:
Title
Percentage of patients who respond to the treatment by day 7.
Description
The primary endpoint will be the percentage of patients who respond to the treatment by day 7. Response will be defined by a drop of >3 points in the lichtiger score and an absolute score <10 on the two prior consecutive days without the need for rescue medications or surgery. In patients who improve and are discharged prior to day 7, the lichtiger score will be calculated based on the two last days of hospitalization, provided that at least 3 days of study medications were dispensed. Patients discharged before 3 days of study medications have been administered will be considered in-eligible and will be dropped out of the analyses.
Time Frame
Day 7

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: UC known and diagnosed by established clinical-endoscopic and histological criteria or newly-diagnosed UC, based on clinical and endoscopic findings, and about to start treatment with corticosteroids. Current hospitalization with Severe UC exacerbation as defined by a Lichtiger score of >10 Age >18 Has not been on oral systemic corticosteroids more than 14 days prior to hospitalization If taking a thiopurine, the dose need to be stable for the last 2 months before admission Exclusion Criteria: Pregnant women Allergy / unable to take prednisone / hydrocortisone/ 5-ASA. Active infection - either enteric or elsewhere Severe renal, liver or cardio respiratory comorbidity Toxic megacolon, or clinical features suggestive of a need for imminent colectomy Treatment with an anti-TNF within the prior 3 months Prior treatment with cyclosporine or tacrolimus within the prior 3 months Alcohol dependency Unable or unwilling to provide informed consent Participating in other clinical trial within the 2 months prior to admission
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
ROBLIN Xavier, MD
Organizational Affiliation
CHU SAINT ETIENNE
Official's Role
Principal Investigator
Facility Information:
Facility Name
Chu Saint Etienne
City
Saint Etienne
ZIP/Postal Code
42100
Country
France
Facility Name
Department of Gastroenterology Venizeleio General Hospital, Leoforos Knosou
City
Heraklion
Country
Greece
Facility Name
Sheba Medical Center
City
Tel HaShomer
State/Province
Ramat-Gan
Country
Israel
Facility Name
Università di Roma Sapienza
City
Rome
Country
Italy
Facility Name
Institute of Gastroenterology and Department of Internal Medicine, Yonsei University College of Medicine
City
Seoul
Country
Korea, Republic of
Facility Name
Zvezdara University Clinical Center, Gastroenterology Department
City
Belgrade
Country
Serbia

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Combination Corticosteroids+5-aminosalicylic Acids Compared to Corticosteroids Alone (for Ulcerative Colitis).

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