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
| Type | Name | Description |
|---|---|---|
| DRUG | MMF | MMF 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.