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Guselkumab to Prevent Crohn's Disease Returning After Bowel Surgery

Follows adults with Crohn's disease treated with guselkumab after bowel surgery.

Plain-language title generated from the registry record
Registry title: An Observational, Multicenter Study to Evaluate the Effectiveness of Guselkumab for the Treatment of Participants With Crohn's Disease After Surgical Resection

Key facts

Where
Shanghai, ChinaSee the site

Where in China

  • Shanghai 10th People's Hospital, Tongji University School of MedicineShanghai, ChinaNo longer taking part

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  2. Are travel costs paid?
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  4. What happens if I want to stop?
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Trial details

Who runs it
Shanghai 10th People's Hospital
Trial code
NCT07528040
Record updated
14 April 2026
Original description
The goal of this single arm ,non-interventional, prospective, descriptive study is to evaluate the efficacy of guselkumab treatment in preventing endoscopic recurrence of Crohn's Disease in adult participants who have a documented diagnosis of moderate to severe CD and have undergone an ileocolonic surgical resection. The primary endpoint is Endoscopic recurrence rate at week24.Read full original descriptionShow less

An Observational, Multicenter Study to Evaluate the Effectiveness of Guselkumab for the Treatment of Participants With Crohn's Disease After Surgical Resection

The goal of this single arm ,non-interventional, prospective, descriptive study is to evaluate the efficacy of guselkumab treatment in preventing endoscopic recurrence of Crohn's Disease in adult participants who have a documented diagnosis of moderate to severe CD and have undergone an ileocolonic surgical resection. The primary endpoint is Endoscopic recurrence rate at week24.

Inclusion: Patients≥ 18,; Have a documented diagnosis of moderate to severe CD; Have undergone an ileocolonic surgical resection.

Exclusion: Has complications of CD, such as short bowel syndrome Currently has or is suspected to have an abscess; Active infection; Currently has a malignancy or has a history of malignancy within 5 years.

ClinicalTrials.gov NCT07528040