Trial Details
AuthorisedBasic Information
| Clinical ID | c5134 |
|---|---|
| Identifier | EUCTR2008-005015-17-NL |
| Trial Title | Effect of N-acetylcysteine on thiopurine related hepatotoxicity in IBD patients - NACTOX |
| Trial URL | Visit Original Page |
Study Information
| Study Results | NULL |
|---|---|
| Conditions | adult patients (18-70 years old) who have been treated with azathioprine, 6-mercaptopure or 6-thioguanine for inflammatory bowel disease, in whom hepatotoxicity occured as an adverse event, are eligible. Prior to definite inclusion, the patients will be s |
| Interventions | Trade Name: acetylcysteineProduct Name: acetylcysteinePharmaceutical Form: Effervescent tabletINN or Proposed INN: ACETYLCYSTEINECAS Number: 616911Concentration unit: mg milligram(s)Concentration type: equalConcentration nu |
Participant Information
| Sponsor | VU university medical centre |
|---|---|
| City | NULL |
| Country/Region | Netherlands |
Enrollment Criteria
| Sex Requirement | NOT SPECIFIED |
|---|---|
| Age Requirement | NULL |
Study Design
| Study Type | Interventional clinical trial of medicinal product |
|---|---|
| Phase | NULL |
Time Information
| Start Date | NULL |
|---|---|
| Primary Completion Date | NULL |
| Completion Date | NULL |