CClinicalTrials.gg
Status unknownNCT02088944Updated Mar 17, 2014

a Single-center Registered Clinical Research of Chinese Patients With Moderate to Severe Crohn's Disease

An observational study in Serological C Reactive Protein or Erythrocyte Sedimentation Rate, sponsored by Nanfang Hospital, Southern Medical University. Status unknown. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2014-03-17.

Sponsored by Nanfang Hospital, Southern Medical University · Observational

The sponsor has not verified this record recently (last verified Mar 2014), so the status shown — last known as Not yet recruiting — may be out of date.
Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
142
Ages
18 Years to 75 Years
Sex
All
01

Study summary

Many studies reveal that infliximab (IFX, an immunoglobulin gamma-1 antibody)can response well to Crohn's Disease(CD) patients who are intolerant of corticosteroids and immunosuppressant,or steroids-dependent .More over,A complex fistula in CD is an indication for early IFX therapy in conjunction with surgical drainage.Some papers claim that IFX may prevent enterectomy CD patients from relapsing. Those with risk factors which at diagnosis associated with " disabling disease "include age \< 40 years, initial need for steroid therapy, and the presence of perianal disease are recommended to use IFX early.

IFX is approved by State Food And Drug Administration(SFDA) in 2007 ,but the safety is still controversial by then.Some studies proclaim that the side effect may be infections,acute infusion reactions,anaphylactic reactions,autoimmunity,drug-induced lupus,congestive heart failure,abortion and demyelination,etc.

So some problems still need to be settled as follows:1)all the the infliximab dates are from other countries,there is rare date from the Chinese,especially the large quantity of random controlled studies and the CD patients with enterectomy.2)despite of the large number of databases from the international ,when to stop and the predictor of the response is still obscure.3)The high cost of IFX may hinder its applications,especially for the moderate to severe active CD patients who take mesalazine and/or immunosuppressant to maintain remission.In addition,the pathogenic age segments in the occurence of CD: from 15\~ 50 years old ,so they suffer from the disability of self-improvements.

The main object of the clinical trial is to complete the database of Chinese CD patients ,especially the safety and efficacy of IFX and those with enterectomy.Then we can record the clinical manifestations of the moderate to severe CD patients with the use of IFX or conventional drugs,including the dose,course and Concomitant treatment.We can also study the predictor and the appropriate time to stop using IFX .We can make the mode of cost-benefit help the patients choose the best project.

02

Conditions studied

  • Serological C Reactive Protein or Erythrocyte Sedimentation Rate
03

In context

Lead sponsor

Nanfang Hospital, Southern Medical University is the lead sponsor of 480 studies on the registry; 212 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

moderate to severe CD patients

Inclusion criteria

  • CD patients excluded from other diseases who are documented diagnosed with the tissue biopsy from colonoscopy or surgery,or those without tissue biopsy are followed over 6-12months finding that the clinical changs are in line with CD.
  • The moderate to severe CD patients (Best Crohn's disease activity index>220)

Exclusion criteria

Exclusion Criteria:

  • Patients who are not willing to anticipate the trial
05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
142 participants (estimated)
Target follow-up
8 Weeks
Patient registry
Yes

Groups and cohorts

  • exposed to IFX

    Drug: Infliximab

Interventions

  • DrugInfliximab
06

What researchers measure

Primary outcomes

  1. CD endoscopic index of severity(CDEIS)<4

    Time frame: 4 years

Secondary outcomes

  1. no endoscopic ulcer

    Time frame: 4 years

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 17, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02088944
Lead sponsor
Nanfang Hospital, Southern Medical University
Responsible party
Sponsor
First posted
Mar 17, 2014
Start date
Mar 2014
Primary completion
Oct 2015 (estimated)
Last update
Mar 17, 2014
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Mar 2014. You cannot join it, but the record below documents what was studied.

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