Evidence map›Paper›PMID 32611737›Full record

ArticleBMJ open2020

Protocol for a multinational risk-stratified randomised controlled trial in paediatric Crohn's disease: methotrexate versus azathioprine or adalimumab for maintaining remission in patients at low or high risk for aggressive disease course.

Rachel E Harris, Marina Aloi, Lissy de Ridder, Nicholas M Croft, Sibylle Koletzko, Arie Levine, Dan Turner, Gigi Veereman, Mattias Neyt, Laetitia Bigot and 3 more

Registry-linked trialOpen access · goldAbstract readClinical Trial Protocol
In one paragraph

Article in BMJ open, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02852694 (Risk-stratified Randomized Controlled Trial in Paediatric Crohn Disease), which is not on this map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 23% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02852694 phase4completednot on this map

Risk-stratified Randomized Controlled Trial in Paediatric Crohn Disease:Methotrexate Vs Azathioprine or Adalimumab for Maintaining Remission in Patients At Low or High Risk for Aggressive Disease Course, Respectively-a Treatment Strategy

TypeinterventionalSponsorPIBD-NetRan2017 to 2021Enrolled192ConditionsCrohn's DiseaseArmsMethotrexate, Adalimumab, Azathioprine / 6 Mercaptopurine
3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Saudi consensus guidance for the diagnosis and management of inflammatory bowel disease in children and adolescents.Saudi journal of gastroenterology : official journal of the Saudi Gastroenterology Association · 2025
    Guideline
  2. Review
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 11 institutions in 9 countries.

Rachel E HarrisDepartment of Paediatric Gastroenterology, Royal Hospital for Children Glasgow, Glasgow, UK.ORCID 0000-0001-6507-3487
Marina AloiPaediatric Gastroenterology and Liver Unit, Sapienza University of Rome, Roma, Lazio, Italy.
Lissy de RidderPaediatrics, Erasmus MC/Sophia Childrens Hospital, Rotterdam, The Netherlands l.deridder@erasmusmc.nl.ORCID 0000-0002-6035-1182
Nicholas M CroftDepartment of Paediatric Gastroenterology, Barts and The London School of Medicine and Dentistry, London, UK.
Sibylle KoletzkoPediatric Gastroenterology and Hepatology, Dr. V. Hauner Children's Hospital, Munich, Germany.
Arie LevineEdith Wolfson Medical Center, Tel Aviv University, Tel Aviv, Israel.
Dan TurnerDepartment of Paediatric Gastroenterology, Hebrew University of Jerusalem, Jerusalem, Israel.
Gigi VeeremanPediatric GI, UZBrussels-VUB, Brussels, Belgium.
Mattias NeytME-TA Medical Evaluation and Technology Assessment, Merendree, Belgium.
Laetitia BigotPIBD-Net, Hôpital universitaire Necker-Enfants malades, Paris, Île-de-France, France.
Frank M RuemmeleService de Gastroentérologie Pédiatrique, Hôpital Universitaire Necker-Enfants Malades, Paris, Île-de-France, France.
Richard K RussellDepartment of Paediatric Gastroenterology, Royal Hospital for Children Glasgow, Glasgow, UK.ORCID 0000-0001-7398-4926
PIBD SETQuality consortium and PIBDnet
Royal Hospital for Children · GBCenter for Assessment · USDélégation Paris 5 · FRErasmus MC - Sophia Children’s Hospital · NLHebrew University of Jerusalem · ILHôpital Necker-Enfants Malades · FRQueen Mary University of London · GBSapienza University of Rome · ITTel Aviv University · ILUniversity of Warmia and Mazury in Olsztyn · PLVictoria University of Bangladesh · BD

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionImmunomodulators such as thiopurines (azathioprine (AZA)/6-mercaptopurine (6MP)), methotrexate (MTX) and biologics such as adalimumab (ADA) are well established for maintenance of remission within paediatric Crohn's disease (CD). It remains unclear, however, which maintenance medication should be used first line in specific patient groups.

aimsTo compare the efficacy of maintenance therapies in newly diagnosed CD based on stratification into high and low-risk groups for severe CD evolution; MTX versus AZA/6MP in low-risk and MTX versus ADA in high-risk patients. Primary end point: sustained remission at 12 months (weighted paediatric CD activity index ≤12.5 and C reactive protein ≤1.5 fold upper limit) without relapse or ongoing requirement for exclusive enteral nutrition (EEN)/steroids 12 weeks after treatment initiation. METHODS AND ANALYSIS: REDUCE-RISK in CD is an international multicentre open-label prospective randomised controlled trial funded by EU within the Horizon2020 framework (grant number 668023). Eligible patients (aged 6-17 years, new-onset disease receiving steroids or EEN for induction of remission for luminal ± perianal CD are stratified into low and high-risk groups based on phenotype and response to induction therapy. Participants are randomised to one of two treatment arms within their risk group: low-risk patients to weekly subcutaneous MTX or daily oral AZA/6MP, and high-risk patients to weekly subcutaneous MTX or fortnightly ADA. Patients are followed up for 12 months at prespecified intervals. Electronic case report forms are completed prospectively. The study aims to recruit 312 participants (176 low risk; 136 high risk). ETHICS AND DISSEMINATION: ClinicalTrials.gov Identifier: (NCT02852694), authorisation and approval from local ethics committees have been obtained prior to recruitment. Individual informed consent will be obtained prior to participation in the study. Results will be published in a peer-reviewed journal with open access. TRIAL REGISTRATION NUMBER: NCT02852694; Pre-results.

Indexed as

AdalimumabAdolescentAnti-Inflammatory AgentsAzathioprineChildCrohn DiseaseFemaleHumansImmunosuppressive AgentsMaintenance ChemotherapyMaleMethotrexateMulticenter Studies as TopicProspective StudiesRandomized Controlled Trials as TopicRemission InductionAdalimumabAnti-Inflammatory AgentsAzathioprineImmunosuppressive AgentsMethotrexateclinical trialsinflammatory bowel diseasepaediatric gastroenterology

Identifiers

PMID32611737
PMCPMC7332179
OpenAlexW3038601097

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.