NIHR CRN: Yorkshire and Humber
York, S10 2SB, United Kingdom
NCT Number: NCT04108637
ALBAMA study is designed to find out if the effects of Penicillin allergy assessment pathway (PAAP) intervention is on penicillin prescribing
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Notify Me18 year and older
All sexes
Interventional
Not applicable
York, S10 2SB, United Kingdom
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
N.B.1 Patients who have been formally tested for penicillin allergy in the past and been found not to be penicillin allergic but still have a medical record indicating a penicillin allergy, are eligible for the trial.
Exclusion criteria
GPs may also want to exclude vulnerable patients who are deemed to be unsuitable to participate for other reasons such as, but not limited to, terminal illness, reliability, mental illness, learning difficulties, anxiety, and other family circumstances.
N.B.1 Patients that are currently taking medicines with antihistamine properties that cannot be temporarily withheld, or patients with isolated dermographism, may still be eligible to participate but will need to be discussed with the research team prior to consent.
N.B.2 Pregnancy and breastfeeding exclusion criteria are only applicable at screening (due to potential risks of PAT); these patients would not need to be withdrawn if in follow up.
Summary of penicillin allergy assessment pathway :
Stage-1 PAAP in Primary Care - Clinical History. Screening, questionnaire and antimicrobial history will be undertaken in primary care Stage-2 Skin Test(ST) in hospital clinic (this may not be needed for all participants) Stage 3 Oral Challenge Test (OCT) in hospital clinic Testing will involve half a day in clinic and then a three-day post clinic course of oral antimicrobial therapy, without a reaction
Other names: PAAP
Time frame: Measured at up to 12 month post-randomisation
The proportion of participants who receive prescriptions for a penicillin when attending for predefined conditions where a penicillin is the first-line recommended antibiotic
Time frame: Measured after first antibiotic prescription, which can occur any time during the follow-up period for patients(Up to 12 months post randomisation)
Treatment "response failure" will be defined as: Re-presentation with worsening or non-resolving symptoms following treatment with an antibiotic up to 28 days after initial antibiotic prescription (including re-prescription of antibiotic within 28 days of an index prescription) for predefined conditions (TPP/notes review), over the year subsequent to randomisation. This will be compared between groups
Time frame: Measured up to 12 month post-randomisation
Duration of symptoms (in days) rated 'moderately bad' or worse by patients, after initiation of antibiotic treatment
Time frame: Measured up to 12 month post-randomisation
Count of total antibiotic use (measured as total number of days therapy and as average daily quantity (ADQ) antibiotics. Total number of penicillin and each non-penicillin antibiotic prescriptions (measured as total number of days therapy and ADQ)
Time frame: Measured up to 12 month post-randomisation
Count of total number of hospital admissions
Time frame: Measured up to 12 month post-randomisation
Count of total length of hospital stays
Time frame: Measured up to 12 month post-randomisation
Mortality rates compared between intervention arms
Time frame: Measured up to 12 month post-randomisation
Total number of patients with MRSA infection/colonisation compared between intervention arms
Time frame: Measured up to 12 month post-randomisation
Number of patients with Clostridium difficile infection
Time frame: Within 12 months of practice recruitment of a proportion of tested patients
GP and patient interviews
Time frame: Within 12 months of practice recruitment of a proportion of tested patients
Change in self-reported behaviour by clinicians and patients.
Time frame: Within 12 months of practice recruitment of a proportion of tested patients
influences on behaviour by clinicians and patients.
Time frame: Collated for period: randomisation to up to 12 months of randomisation
Measurement of quality adjusted life years in each arm
Time frame: check performed at 3 and 12 months
The proportion of ALABAMA participants whose labels were removed and remain removed from the medical eHR
Time frame: Measured at up to 12 month post-randomisation
A descriptive analysis will be performed looking at the safety (number of AEs and SAEs) of de-labelling in the intervention group
Time frame: Measured at the end of the study
Descriptive analysis using data captured in the notes review CRF
University of Leeds
Other
Penicillin Allergy Status And Its Effect On Antibiotic Prescribing, Patient Outcomes, and Antimicrobial Resistance
Acronym: ALABAMA
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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