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Completed

NCT Number: NCT04454229

The Use of Penicillin Allergy Clinical Decision Rule to Enable Direct Oral Penicillin Challenge

Whilst validated tools exist to enable inpatient penicillin assessment and de-labelling, limited evidence is available regarding the safety and efficacy in the outpatient clinic. The ability to deliver point-of-care penicillin allergy testing for a large cohort of patients, without skin testing, will improve patient access to testing and utilization of preferred penicillin antibiotics.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Austin Health, Heidelberg, Victoria, Australia

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About this study

Patient-reported penicillin allergies result in poor health outcomes for patients and drive inappropriate antibiotic prescribing, antimicrobial resistance and healthcare costs. Our group has internally and externally validated a novel penicillin allergy clinician decision rule (PEN-FAST) that is able to identify low risk penicillin allergies with a negative predictive value of 96% (95%; 94-98%). Therefore, whilst validated tools exist to enable inpatient penicillin assessment and de-labelling, limited evidence is available regarding the safety and efficacy in the outpatient clinic. The ability to deliver point-of-care penicillin allergy testing for a large cohort of patients, without skin testing, will improve patient access to testing and utilization of preferred penicillin antibiotics.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult patients referred to the outpatient allergy clinic for a penicillin allergy history;
  • Willing and able to give consent.

Exclusion criteria

  • Patient age is < 18 years;
  • Patients with a PEN-FAST score less than 3
  • Pregnancy;
  • Any other illness that, in the investigator's judgement, will substantially increase the risk associated with subject's participation in this study;
  • Patients with history of type A adverse drug reaction, drug-associated anaphylaxis, idiopathic urticaria/anaphylaxis, mastocytosis, serum sickness, blistering skin eruption or acute interstitial nephritis;
  • Patients where the allergy history was not able to be confirmed with patient;
  • Patients on concurrent antihistamine therapy;
  • Patients receiving more than stress dose steroids (i.e. > 50mg QID hydrocortisone [or steroid equivalent]).

Treatment and study plan

Direct oral penicillin challenge

Other

The patient will receive a single dose of oral penicillin, following baseline vital signs.

Standard of care

Other

Routine management as per the treating clinicians that include skin prick and intradermal beta-lactam testing, followed by oral penicillin challenge in the setting of negative skin testing.

Primary outcomes

  1. The difference in the proportion of positive oral challenges (i.e. immune-mediated reaction)

    Time frame: up to 48H after oral challenge

Secondary outcomes

  1. Proportion of patients referred to the outpatient allergy clinic that are eligible for intervention (i.e randomization) as per protocol [Eligibility to screened ratio]

    Time frame: Before randomization

  2. Feasibility of recruitment defined as the proportion of patients consenting to participate in the study as per protocol from eligible patients. [Recruitment to eligibility ratio].

    Time frame: Before randomization

  3. Feasibility of intervention delivery defined as the proportion of patients randomized to the intervention arm who had the intervention delivered as per protocol. [Intervention to recruitment ratio]

    Time frame: Before randomization

  4. The proportion of patients with a penicillin allergy who experience an antibiotic associated immune mediated adverse event OR severe adverse drug reaction as per protocol definitions.

    Time frame: Up to 48h after the drug challenge

  5. The proportion of patients with a penicillin allergy who experience an antibiotic associated non-immune mediated adverse event.

    Time frame: Up to 48h after the drug challenge

  6. The proportion of patients that will respect the protocol (protocol compliance)

    Time frame: Up to 48h after the drug challenge

  7. Proportion of patient with positive Penicillin Skin Testing

    Time frame: Up to 48h after the drug challenge

  8. Proportion of patients with non-immune mediated positive oral provocation

    Time frame: Up to 48h after the drug challenge

  9. Proportion of patients with severe adverse reaction - anaphylaxis/death

    Time frame: Up to 48h after the drug challenge

  10. Time from randomization to delabelling

    Time frame: Up to 48h after the drug challenge

  11. Number of appointments required for Penicillin delabelling

    Time frame: Up to 48h after the drug challenge

  12. Assessment with the Pre-Questionnaire and the 6 months follow-up Questionnaire

    Time frame: Up to 6 months after the drug challenge

Sponsors and collaborators

Lead sponsor

Austin Health

Other Gov

Registry information

Official study title

The Use of Penicillin Allergy Clinical Decision Rule to Enable Direct Oral Penicillin Challenge - An International Multicenter Randomized Control Trial - The PALACE Study

Acronym: PALACE

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Jul 1, 2020
Registry last updated
Mar 6, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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