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NCT Number: NCT07833293

Effectiveness of AI-Assisted Antibiotic Prescribing

This randomized controlled trial aims to evaluate the impact of providing LLM access to physicians on antibiotic prescribing appropriateness, using a composite outcome instrument, the Antibiotic Prescribing Appropriateness Score (APAS), that simultaneously evaluates antibiotic selection, dosing, duration, clinical reasoning, and management planning. Participants will be randomly assigned to one of two groups: the intervention group will have access to an LLM alongside conventional resources, while the control group will use conventional resources only (e.g. UpToDate, PubMed and Google Search with AI features disabled). Both groups will respond to a set of clinical vignettes covering common infectious disease scenarios requiring antibiotic prescribing decisions, with responses evaluated using an expert-validated grading rubric and independently scored by blinded raters.

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Key information

Conditions

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

Inappropriate antibiotic prescribing remains one of the most consequential drivers of antimicrobial resistance globally, with particular urgency in low- and middle-income countries, where regulatory enforcement, antibiogram coverage, and specialist infectious-disease support are limited. Recent advances in Large Language Models (LLMs) have shown promise in supporting clinical decision-making. LLMs have been explored as tools for synthesizing antibiotic recommendations and flagging spectrum mismatches. Yet LLMs may produce confident but incorrect recommendations, and their use may reduce the quality of physicians' own clinical reasoning through over-reliance. Whether this promise translates into measurably better antibiotic prescribing behavior among practising physicians, measured across the full spectrum of selection, dosing, and clinical reasoning, has not been rigorously evaluated in a randomized, controlled setting.

This study evaluates whether access to an LLM affects the Antibiotic Prescribing Appropriateness Score (APAS) among licensed physicians in Pakistan. Secondary objectives include assessing whether the intervention improves antibiotic selection and spectrum-matching, whether the effect differs by physician clinical experience, and whether LLM access affects the time physicians spend per vignette.

This study will be an assessor-blind, randomized controlled trial with two arms. Participants will be randomly assigned to either the intervention or control arm in a 1:1 ratio. Outcome assessors (those scoring the APAS responses) will be blinded to participants' group assignments and will evaluate vignette responses without knowledge of which arm the responding physician was in. Each participant is expected to complete 6-10 vignettes in a single, proctored, 75-minute session. The order of vignettes will be randomized independently for each participant to control for order effects. The time spent on each vignette will be automatically recorded.

In the intervention arm, participants will have access to ChatGPT in addition to conventional diagnostic and reference resources (UpToDate, PubMed, Google search with AI features disabled). In the control arm, participants will use conventional resources only (UpToDate, PubMed, Google Search with AI features disabled). Both arms will evaluate the same set of clinical vignettes.

Participants will be presented with clinical vignettes covering common infectious disease scenarios requiring antibiotic prescribing decisions. Vignettes will be sourced and modified based on clinically realistic cases relevant to the target population, and will follow a standardized format, including the patient's chief complaint and history of present illness, and physical examination findings.

Vignettes will cover a range of infectious disease presentations encountered in family medicine, general practice, internal medicine, and emergency medicine, avoid overly rare or highly specialized conditions, and reflect a range of prescribing decisions, including empiric treatment, culture-directed de-escalation, spectrum selection, dosing decisions, and stewardship-sensitive presentations in which withholding antibiotics may be the clinically correct decision, to avoid reward bias toward prescribing. All vignettes will be developed by an independent expert panel, and each vignette will be accompanied by an expert-validated grading rubric specifying expected answers for antibiotic selection, dosing, route, and duration, clinical reasoning, and management planning.

The primary measure of prescribing appropriateness will be the APAS, a four-domain rubric scored out of 10 points per vignette and expressed as a percentage. The adjusted mean difference in vignette-level APAS between the intervention and control arms is the primary outcome of our study. Responses will be independently evaluated by three qualified raters blinded to participant identity and treatment assignment. The arithmetic mean of the three raters' total scores will constitute the vignette-level APAS used in the primary analysis.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Completed Bachelor of Medicine, Bachelor of Surgery (MBBS) or equivalent degree. The equivalent degree of MBBS in the US and Canada is Doctor of Medicine (MD).
  • Full or Provisionally Registered Medical Practitioners with the Pakistan Medical and Dental Council (PMDC).

Exclusion criteria

  • Any other Registered Medical Practitioner (Full or Provisional) with PMDC not holding an MBBS or equivalent degree (e.g., practitioners with a Bachelor of Dental Surgery (BDS)).

Treatment and study plan

ChatGPT

Other

Participants in the intervention arm will have access to ChatGPT in addition to conventional diagnostic and reference resources.

Primary outcomes

  1. Antibiotic Prescribing Appropriateness Score (APAS)

    Time frame: Assessed at a single time point for each case, during the scheduled diagnostic reasoning evaluation session, which takes place between 0-6 days after participant enrollment.

    The primary outcome will be the composite score (expressed as a percentage) based on an expert-validated rubric that evaluates physician responses across four domains for each clinical vignette: Antibiotic Selection & Spectrum (0-6 points), Dosing, Route & Duration (0-3 points), Clinical Reasoning (0-2 points), and Management Plan (0-2 points). The total score for each vignette is the sum of scores across the four domains (maximum 13 points). APAS is expressed as a percentage, calculated as the total score divided by 13, multiplied by 100. The primary endpoint is vignette-level APAS. Responses will be independently evaluated by three licenses physicians blinded to participant identity and treatment assignment. The arithmetic mean of the three raters' total scores will constitute the vignette-level APAS used in the primary analysis.

Secondary outcomes

  1. Antibiotic Selection, Spectrum & Dosing Subscore

    Time frame: Assessed at a single time point for each case, during the scheduled diagnostic reasoning evaluation session, which takes place between 0-6 days after participant enrollment.

    The antibiotic selection, spectrum, and dosing elements of APAS (0-6 points per vignette, expressed as a percentage), scored using the same rubric as the primary outcome.

  2. Time per Vignette

    Time frame: Assessed at a single time point for each case, during the scheduled diagnostic reasoning evaluation session, which takes place between 0-6 days after participant enrollment.

    We will compare how much time (in seconds) participants spend per case between the two study arms.

Study contacts

Contact information is provided by the study sponsor or research team.

Ihsan Ayyub Qazi

CONTACT

[email protected]

+92 42 35608368

Sponsors and collaborators

Lead sponsor

Lahore University of Management Sciences

Other

Collaborators

  • King Abdullah University of Science and Technology

Registry information

Official study title

Effectiveness of AI-Assisted Antibiotic Prescribing: A Randomized Controlled Trial

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Sep 22, 2026
Registry last updated
Sep 22, 2026

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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