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Single step oral provocation challenge in children with a low risk reported penicillin allergy (Safe-Step): a prospective study.

The safety and efficacy of a single step oral provocation challenge in children with a low risk reported penicillin allergy (Safe-Step): a prospective study.

Status
Not yet recruiting
Phases
Phase 3
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12625000359437
Acronym
One-Step
Enrollment
500
Registered
2025-04-24
Start date
2025-05-05
Completion date
Unknown
Last updated
2025-09-08

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

Conditions

None listed

Brief summary

This study seeks to establish a safe, one-step oral provocation challenge pathway for children with penicillin allergies. To be eligible, children must have experienced a low-risk initial reaction, such as a mild rash or a delayed urticarial rash. The goal of this approach is to inform primary shared care pathways for conducting penicillin testing in children within the community.

Interventions

This prospective study will evaluate the outcomes of a single-dose oral provocation challenge in paediatric participants with a reported low-risk penicillin allergy. The one stage oral challenge will be undertaken as follows; the dose will be calculated in mg/kg according to the patient's weight and in accordance with the Australian Medicines Handbook paediatric dosage guidelines for the relevant penicillin. The dose will then be administered as either an oral tablet or an oral liquid, dependen

This prospective study will evaluate the outcomes of a single-dose oral provocation challenge in paediatric participants with a reported low-risk penicillin allergy. The one stage oral challenge will be undertaken as follows; the dose will be calculated in mg/kg according to the patient's weight and in accordance with the Australian Medicines Handbook paediatric dosage guidelines for the relevant penicillin. The dose will then be administered as either an oral tablet or an oral liquid, dependent on patient preference or dose dependent. In order to ensure adherence, these doses will be administered under direct supervision to ensure adherence. For the five-day extended course, the dose will be calculated as above and administered twice daily as observed by parents. and will be administered as either an oral tablet or an oral liquid, dependent of patient preference or dose dependent. There will be follow up via telephone on day 2 and say 7 of the five-day courses, to monitor adherence. As part of routine care, the study team will review patients at the Drug Allergy Clinic, gathering relevant data from their history, medical notes, and antibiotic allergy details. This includes the type and severity of the reaction, timing of the reaction, the interval between the dose administered and the reaction, any underlying illnesses or medications at the time of the reaction, route of administration, past and current medical history, family history of allergies or co-morbidities, and the management of both acute and post-reaction phases. This information will be included in the analysis. Eligible participants will be contacted by the study team—either during their initial consultation or via telephone call following the consultation—to invite them to participate in the study. Consented participants will then undergo a one-stage oral provocation challenge, where they will receive 100% of the calculated daily dose of penicillin based on their weight and age. Following the challenge, they will be observed for one hour in the hospital according to the Australian Society of Clinical Immunology and Allergy consensus guidelines. If no immediate reaction is observed, participants will then receive a five-day extended course of penicillin, which is the current standard clinical care. Upon discharge, parents will be provided with an updated, approved health information sheet, which includes detailed information on potential types of reactions, their management, and the proper steps to take if a reaction occurs. The sheet also contains contact information for families to reach out if they have concerns or notice any signs of a reaction. Additionally, an email address will be provided for families to share any relevant details or photos related to a reaction. Follow-up will take place on Day 2 and Day 7 after the initial challenge. The Day 2 phone call aims to establish contact with the family and ensure that the child is tolerating the extended treatment course without any issues. The Day 7 call is to confirm that the child has completed the course successfully and has not experienced any delayed reactions within the 48-hour post-treatment window. This allows us to update the Drug Allergy Notification, either removing the allergy label or confirming the allergy if a reaction has occurred.

Sponsors

WA Health
Lead SponsorHospital

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Diagnosis
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
6 Months to 18 Years
Healthy volunteers
No

Inclusion criteria

Children and young adults, male or female, aged 6 months to 18 years of age (inclusive) who have been assessed through the Drug Allergy Service with a self-reported beta-lactam penicillin allergy, with a low-risk history of a delayed non-urticarial rash who are willing to take part in this study. Low risk reported allergy is defined by mild, delayed, non-urticarial, macula/popular, or erythemous rash, mild gastro-intestinal symptoms or family history only

Exclusion criteria

• Females who are pregnant (Pregnancy tests will be offered to sexually active females and can be performed on the day of challenge) • Families with the inability to give informed consent based on language barriers requiring an interpreter. (These patients will be challenged through the normal challenge clinics as per standard clinical care and therefore not disadvantaged) • Non-beta-lactam antibiotic allergies • Patients with a reported immediate IgE mediated reaction to a penicillin • Patients with a reported history of a reaction to a beta-lactam cephalosporin. • Severe cutaneous adverse reactions • Type II-IV allergies (Serum sickness, Stevens-Johnson Syndrome (SJS), Toxic epidermal necrolysis (TEN), Acute interstitial nephritis (AIN), Drug rash eosinophilia syndrome (DRESS), Acute generalised Exanthematous Pustulosis (AGEP), Haemolytic anaemia)

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026