Skip to content

Study of safety and immunogenicity of Measles vaccine (Rouvax®) administered by transcutaneous route (France)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN88861431
Enrollment
Unknown
Registered
2005-11-25
Start date
2004-03-23
Completion date
Unknown
Last updated
2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Vaccine/immunisation Infections and Infestations Vaccination

Interventions

Intervention: 1 dose of Rouvax® vaccine administered to the skin of the shoulder after stripping (abrading) the skin Control: 1 dose of Rouvax® administered by injection

Sponsors

World Health Organization (WHO)/Department of Immunisation, Vaccines and Biologicals (IVB) (Switzerland)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Healthy adults between 18 and 22 years of age of haplotype HLA-A201 who have previously been immunised against measles and for whom the anti-measles antibodies are low 2. Female participants must be under contraception

Exclusion criteria

Exclusion criteria: 1. Previous infection with measles 2. Contra-indications to the use of Rouvax® vaccine 3. Hypersensitivity to egg proteins 4. Human Immunodeficiency Virus (HIV) seropositive 5. Treatment with corticosteroids or immunosuppressors in 15 days prior to enrolment 6. Exposure of back-skin to sun in 15 days prior to enrolment 7. Dermatological pathology on back 8. Acute and evolutive disease 9. Blood donation in three months prior to enrolment 10. In a period of exclusion following previous clinical trials 11. Having received 3800 or more Euros in preceeding 12 months from participation in clinical trials

Design outcomes

Primary

MeasureTime frame
Not provided at time of registration

Secondary

MeasureTime frame
Not provided at time of registration

Countries

France

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026