Trial Details
RecruitingBasic Information
| Clinical ID | c5532 |
|---|---|
| Identifier | NL-OMON21974 |
| Trial Title | Effect of N-acetylcysteine on thiopurine related hepatotoxicity in IBD patients. |
| Trial URL | Visit Original Page |
Study Information
| Study Results | NULL |
|---|---|
| Conditions | Inflammatory bowel disease; IBD; Crohn's disease; de ziekte van Crohn; ulcerative colitis; colitis ulcerosa; thiopurines; oxidative stress; hepatotoxicity; levertestafwijkingen |
| Interventions | Continuation of thiopurine treatment during eight weeks. During four weeks 600mg N-acetylcysteine effervescent tablets four times daily. |
Participant Information
| Sponsor | VU University Medical Center |
|---|---|
| City | NULL |
| Country/Region | NULL |
Enrollment Criteria
| Sex Requirement | NOT SPECIFIED |
|---|---|
| Age Requirement | NULL |
Study Design
| Study Type | Interventional |
|---|---|
| Phase | NULL |
Time Information
| Start Date | NULL |
|---|---|
| Primary Completion Date | NULL |
| Completion Date | NULL |