Actively Recruiting
Jack Jumper Ant Venom Immunotherapy Long-term Effectiveness Investigation
Led by Murdoch Childrens Research Institute · Updated on 2026-03-31
100
Participants Needed
3
Research Sites
200 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Jack Jumper ant (JJA) venom allergy is a uniquely Australian medical condition. It is the leading cause of venom allergy and affects up to three per cent of the population. 70 percent of people with JJA allergy will have another reaction on a repeat sting and this sensitivity appears to persist for many years. Venom immunotherapy (VIT) has been shown to be a safe and effective treatment in the prevention of severe systemic allergic reactions (anaphylaxis) to future stings. It is currently offered to patients as standard care in Tasmania, South Australia and Victoria. However, whilst JJA VIT has been used for many years, there is a lack of evidence on the long-term benefit of the treatment and how it impacts patient quality of life. This trial will offer patients who have completed a JJA VIT program (between 3 and \< 6-years duration) and have been off-treatment for at least 18-months and \< 5 years, to have a supervised JJA sting challenge and blood test to assess their JJA venom tolerance level. It will also ask them to complete a set of questionnaires at different timepoints to obtain a history of their exposure and reactions to JJA stings outside of the hospital setting (field stings), and to measure the impact of the completed VIT and knowledge of their sting challenge outcome on their quality of life and their behaviours around auto-injectors. These measures will be used to explore the long-term effectiveness of JJA VIT and the impact of a sting challenge post VIT on a patient's quality of life.
CONDITIONS
Official Title
Jack Jumper Ant Venom Immunotherapy Long-term Effectiveness Investigation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 years or older who have completed a continuous Jack Jumper Ant Venom Immunotherapy program lasting between 3 and less than 6 years
- Completed the immunotherapy treatment at least 18 months ago but less than 5 years ago
- Ability to provide informed consent
You will not qualify if you...
- Persons under 18 years of age
- Adults who have not completed a continuous immunotherapy program lasting between 3 and less than 6 years
- Adults who stopped immunotherapy less than 18 months ago or more than 5 years ago
- Individuals with medical conditions that may increase risk during a sting challenge as judged by the investigator
- Inability to understand study requirements or provide informed consent
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 3 locations
1
Royal Adelaide Hospital
Adelaide, South Australia, Australia, 5000
Actively Recruiting
2
Royal Hobart Hospital
Hobart, Tasmania, Australia, 7000
Actively Recruiting
3
Monash Medical Centre
Clayton, Victoria, Australia, 3168
Actively Recruiting
Research Team
N
National Allergy Centre of Excellence
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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