PneuMum: Pneumococcal Vaccination of Australian Indigenous Mothers to See if it Protects Their Babies From Ear Disease
Sponsored by University of Melbourne
About this trial
Last updated 18 years ago
Study ID
2 November 2005
Status
Unknown status
Type
Interventional
Phase
Phase 3
Placebo
No
Accepting
16 to 39 Years
Female
Trial Timing
Ended 17 years ago
What is this trial about?
PneuMum is a randomised controlled trial that aims to find out if pneumococcal vaccination
for Australian Indigenous mothers, in the last few months of pregnancy or at delivery, can
prevent ear disease in infants. Mothers will receive the 23 valent pneumococcal
polysaccharide vaccine (23vPPV) either: a) during the third trimester of pregnancy; b) soon
after child birth; or c) seven months after child birth (control group). The adult
diphtheria, tetanus and acellular pertussis vaccine (dTPa) will be used as the control
vaccine for the birth dose.
The study aims to recruit 210 Indigenous women aged 18-39 years who have an uncomplicated
pregnancy. Following recruitment, subjects will be randomly assigned to one of the three
groups.
Each mother and infant will be followed from pregnancy until the baby is seven months of age.
Children will receive all of their routinely recommended vaccinations in accordance with the
standard vaccination schedule.
The primary outcome will be prevalence of ear infection at seven months of age, defined as
middle ear effusion or tympanic membrane perforation or acute otitis media. Pneumatic
otoscopy, video-otoscopy and tympanometry will be used in the ear examinations. The primary
analyses will be a direct comparison of the proportion of infants in the control group who
have nasopharyngeal carriage of vaccine type pneumococci at seven months of age compared to
infants in each of the other two groups and a similar comparison of the proportion with
middle ear disease.
What are the participation requirements?
Inclusion Criteria
- Singleton uncomplicated pregnancy
- Reside in Darwin, Maningrida, Wadeye or the Tiwi Islands
- Intends to deliver child at the Royal Darwin Hospital
- Has given informed consent to participate
Exclusion Criteria
- Had 23vPPV within the previous three years
- Had a previous dose of dTpa
- intends to leave the study area during the follow-up period
- HIV positive
- History of severe allergy, uncontrolled asthma or splenectomy