Trial Details
RecruitingBasic Information
| Clinical ID | c5555 |
|---|---|
| Identifier | NL-OMON25639 |
| Trial Title | Title *.Vaccinations in Immunocompromised Patients, Rabies Antibody Response after pre exposure prophylaxis - The VIPRAR study. |
| Trial URL | Visit Original Page |
Study Information
| Study Results | NULL |
|---|---|
| Conditions | Auto-immune diseases (Inflammatory bowel disease/rheumatoid arthritis) |
| Interventions | We offer all eligible ICPs a three-dose rabies PrEP schedule on days 0, 7 and 21-28 intramuscularly, according to the current WHO guidelines for ICPs. At month 12, a 2-dose rabies PEP schedule will be administered intramuscularly at day 0 and day 3. S |
Participant Information
| Sponsor | The International Society of Travel Medicine (ISTM) |
|---|---|
| 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 |