Clinical Trials Directory

Trials / Completed

CompletedNCT04990245

pAtient rePorted Outcomes Linked With histoLogy in Patients With uLcerative cOlitis

APOLLO Study: pAtient rePorted Outcomes Linked With histoLogy in Patients With uLcerative cOlitis

Status
Completed
Phase
Study type
Observational
Enrollment
86 (actual)
Sponsor
Imelda GI Clinical Research Center · Academic / Other
Sex
All
Age
16 Years
Healthy volunteers
Not accepted

Summary

Background and rationale: In ulcerative colitis, treating beyond endoscopic healing has shown a reduction of relapse and hospitalization, pushing for histological remission in daily clinical practice.1 However, very little is known on how histological remission is associated with patient reported outcomes (PROMs).2,3 In recent years, several questionnaires have been developed to assess what really matters to patients: symptoms and the burden UC exerts on them.4 As PROMs are getting more and more attention during drug development programs and drug approval by international organizations, including FDA and EMA, the link between objective outcome measures (endoscopic, histological, biochemical) and PROMs should therefore be better characterized. Objectives and design: To investigate prospectively the association of patient reported outcomes (PROMs) and biochemical, endoscopic and histological outcome measures in patients with ulcerative colitis.

Detailed description

After informed consent, patients will undergo endoscopic assessment evaluating endoscopic disease activity using established scoring systems * Mayo endoscopic sub-score5 * Ulcerative Colitis Endoscopic Index of Severity \[UCEIS\]6 All endoscopic assessments will be recorded, allowing blinded scoring by independent endoscopists afterwards. Study protocol APOLLO - 2 During endoscopy, colonic biopsies will be taken according to standard of care from the most inflamed area of the colon and normal area if applicable, 0-60cm from the anal verge. All biopsies will be scored histologically using the Nancy Index.7 During the same study visit, clinical symptoms (Simple clinical colitis activity index \[SCCAI\]) and patient reported outcomes (PROMs) will be evaluated digitally using validated scoring systems8 * IBD disk * PRO-2 * Visual Analogue Scale * IBD control in case of non-remission Finally, patients will be biochemically (C-reactive protein, hemoglobin, albumin) evaluated, including measurement of drug level (infliximab, adalimumab, vedolizumab) in case of ongoing exposure to biological agents. All evaluations are part of standard-of-care. Definitions * Endoscopic remission: Mayo endoscopic sub-score 0 AND UCEIS 0 * Endoscopic response according to * Mayo score: decrease in Mayo endoscopic sub-score ≥ 1 * UCEIS: decrease in UCEIS ≥ 2 * Endoscopic improvement: Mayo endoscopic sub-score 1 * Histological remission: Nancy histological index 0 * Absence of active/acute histological inflammation: Nancy histological index 0-1 * Histological response: Nancy histological index \> 1 * PRO2 remission: stool frequency ≤ 1 (absolute stool frequency ≤ 3 OR 1-2 stools more than usual) AND rectal bleeding score of 0 (average of 3 days prior to endoscopy) * IBD disk remission per item: * Abdominal pain * Regulating defecation * Interpersonal interactions * Education and work * Sleep * Energy * Emotions * Body Image * Sexual function * Joint pain

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTendoscopic biopsiespatients with planned endoscopy for ulcerative colitis have endosocpic data recorded aswell as biopsy sampling and blood tests

Timeline

Start date
2020-07-01
Primary completion
2021-07-28
Completion
2021-07-28
First posted
2021-08-04
Last updated
2021-08-04

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT04990245. Inclusion in this directory is not an endorsement.