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NCT01906853CompletedPhase 3

Melbourne Infant Study - Bacille Calmette Guérin (BCG) for Allergy & Infection Reduction

A Randomised, Controlled Trial to Determine if BCG Immunisation at Birth Reduces Allergy and Infection in Infants

Source: ClinicalTrials.gov · Last updated 17 Feb 2025

Brief summary (registry, in English)

1. To determine if BCG immunisation at birth, compared to no BCG immunisation, leads to a reduction in measures of allergy and infection in the first 12 months of life. 2. To evaluate the immunological mechanisms underlying the non-specific effects of BCG by comparing markers of immunity between the BCG and non-BCG groups.

Status (registry)
Completed
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
1272 (actual)
First submitted
21 Jul 2013
Start date
Jul 2013
Primary completion date
Sept 2023
Lead sponsor
Murdoch Childrens Research Institute
NCT number
NCT01906853

What you commit to

  • Study type: Interventional · Phase 3
  • Participants enrolled: 1272
  • From Jul 2013 to the primary completion date, Sept 2023
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Treatment with corticosteroids or other immunosuppressive therapy, including monoclonal antibodies against tumour necrosis factor-alpha (TNF-alpha) (e.g. infliximab, etanercept, adalimumab).
  • Born to a mother treated with bDMARDS (e.g. TNF-alpha blocking monoclonal antibodies) in the 3rd trimester;

Other illness

  • Any indication for BCG immunisation in the first 12 months of life including:
    • likely travel to a high tuberculosis (TB) incidence country in the first year of life.
    • Aboriginal and Torres Strait Islander babies living in parts of Australia where the incidence of TB is higher
    • newborn babies, if either parent has leprosy or a family history of leprosy
    • newborn in contact with a patient with TB.
  • Known or suspected HIV infection
  • Malignancies involving bone marrow or lymphoid systems;
  • Serious underlying illness including severe malnutrition;
  • Generalised septic skin disease and skin conditions such as eczema, dermatitis and psoriasis;
  • Significant febrile illness;
  • Family history of immunodeficiency;

Other

  • Congenital cellular immunodeficiencies including specific deficiencies of the interferon gamma pathway;
  • Medically unstable;
  • Mother immunosuppressed;
  • Consanguineous parents;
  • Multiple births more than twins.

Who the study is looking for

  • Less than 10 days old;
  • English speaking mother;
  • An informed consent form must be signed and dated by their parent(s) or legally acceptable representative after the nature of the study has been explained and prior to any study assessments/procedures;
  • The infant's mother has screened negative for HIV during this pregnancy;
  • Born no earlier than eight weeks before estimated date of delivery;
  • Birth weight \>1500g.
  • The legal guardian expects to be able to complete four online/phone questionnaires over the infant's first 12 months of life and for the infant to be available for skin prick testing at RCH between 12-16 months of age.

Age in the registry: - to 10 days · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Mercy Hospital for Women
Coordinator of this site? Confirm its status
HeidelbergAustraliaUnknown status
Royal Children's Hospital
Coordinator of this site? Confirm its status
MelbourneAustraliaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.