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Trials / Recruiting

RecruitingNCT05951517

Mycophenolate Mofetil in Gastrointestinal Henoch-Schonlein Purpura

The Clinical Study of Mycophenolate Mofetil in Pediatric Refractory Gastrointestinal Henoch-Schonlein Purpura

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
24 (estimated)
Sponsor
Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University · Academic / Other
Sex
All
Age
3 Years – 18 Years
Healthy volunteers
Not accepted

Summary

Henoch Schönlein purpura (HSP) is the most common type of vasculitis in children, with an incidence of \~10/100,000, whereas \>90% of the patients develop symptoms at \<10 years of age. Although HSP is generally a self-limiting disease, it may also lead to severe complications, such as intestinal intussusception, infarction and perforation, as well as end-stage renal disease. The management of HSP includes symptomatic treatment and immunosuppressive therapy in certain patients. Previous retrospective studies have reported that most patients with gastrointestinal (GI) symptoms may benefit from early usage of glucocorticoid, whereas there are still a part of HSP patients with GI did not achieved remission after administering of steroid. Therefore, the aim of the present study was to investigate the clinical features of refractory GI HSP and the clinical outcome of mycophenolate mofetil in these patients.

Detailed description

the aim of the present study was to investigate the clinical features of refractory GI HSP and the clinical outcome of mycophenolate mofetil in these patients.

Conditions

Interventions

TypeNameDescription
DRUGMMFMMF treat refractory gastrointestinal Henoch-Schönlein purpura

Timeline

Start date
2023-01-01
Primary completion
2026-12-31
Completion
2026-12-31
First posted
2023-07-19
Last updated
2023-07-19

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05951517. Inclusion in this directory is not an endorsement.