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Trial · NCT07424040

The Efficacy and Safety of Infliximab Combination With Azathioprine in Crohn's Disease in Children

NCT07424040, Not applicable, Not yet recruiting, The Children's Hospital of Zhejiang University School of Medicine

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. The Efficacy and Safety of Infliximab Combination With Azathioprine in Crohn's Disease in Children. Trials, record NCT07424040. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07424040

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
The Efficacy and Safety of Infliximab Combination With Azathioprine in Crohn's Disease in Children
NCT number
NCT07424040
Status
Not yet recruiting
Phases
Not applicable
Enrollment
154 participants, estimated
Lead sponsor
The Children's Hospital of Zhejiang University School of Medicine
Conditions
Crohn's Diseases, Crohn's Disease in Pediatric Patient
Interventions
Infliximab combined with azathioprine therapy, Infliximab monotherapy
First posted
2026-02-20
Last updated
2026-02-20

Source ClinicalTrials.gov

Registered outcomes4

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryThe clinical remission rates((Pediatric Crohn's Disease Activity Index)in the 14th week and the 54th weekthe 14th week and the 54th weekThe clinical remission rateS of the children was evaluated using the PCDAI (Pediatric Crohn's Disease Activity Index). PCDAI\<10 was considered as clinical remission.
SecondaryComparison of adverse reactions between the two treatment regimens within 54 weekswithin 54 weeks
Adverse reactions include infections, tumors, liver and kidney function impairments, myocardial damage, and bone marrow transplantation, etc Compare the incidence rates of adverse reactions between the two groups。
SecondaryThe mucosal healing rates (Simple Endoscopic Score for Crohn's Disease)in the 14th week and the 54th weekthe 14th week and the 54th weekThe SES-CD(Simple Endoscopic Score for Crohn's Disease)obtained under colonoscopy was used to evaluate the condition of mucosal healing. SES-CD\<3 was defined as mucosal healing.
SecondaryPatient-reported outcomes(PRO2) for the 14th week and the 54th weekthe 14th week and the 54th week
The patient-reported outcomes for Crohn's disease use standardized assessment tools, namely the PRO2 scale, which includes two core symptoms: "abdominal pain" and "frequency of defecation". The minimum and maximum values of the PRO2 scale are 0 and above 30 respectively. Higher scores mean a worse outcome.

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
37004887BACKGROUND

Source PubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT07424040

GET https://conductscience.org/api/trials/v1/NCT07424040/registered