RecruitingPhase 3NCT06472219

PREDICATE Trial For Respiratory Tract Infections

Early Prednisolone for Suspected Community-acquired Acute Respiratory Tract Infection (PREDICATE): A Double-blind, Randomised, Multi-centre, Adaptive Platform, Controlled Trial


Sponsor

The University of Hong Kong

Enrollment

1,300 participants

Start Date

Dec 23, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

Background The goal of this clinical trial is to learn if prednisolone works to treat moderate to severe respiratory tract infections in adults admitted to hospital. It will also learn about the safety of prednisolone in this context. The main questions it aims to answer are: Does prednisolone lower the number of participants who develop sepsis or who survive? What medical problems do participants have when taking prednisolone? Researchers will compare prednisolone to a placebo (a look-alike substance that contains no drug) to see if prednisolone works to treat respiratory tract infections in adults. Participants will: Take prednisolone 30mg or a placebo every day for 5 days. Complete a daily diary of symptoms for 30 days and have telephone follow up. Investigators propose to recruit 1300 patients, 650 in each group. The Trial will be conducted in the Emergency Departments and wards of hospitals in Hong Kong. Investigators expect the proportion of patients admitted to the hospital who develop sepsis or who die within 30 days to be reduced from 25% to 18% after taking active treatment. Secondly, investigators expect any difference in the proportion of patients with Serious adverse events(SAEs) not to exceed 5% between active treatment group and control. Benefits to Hong Kong and Worldwide: Active treatments (e.g. prednisolone are cheap, HK$0.2 per 5mg tablet) are widely available across the world. Any reduction of progression to sepsis and death if applied worldwide would improve the lives of millions of patients and save millions of dollars of healthcare costs.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a personalized treatment approach for adults hospitalized with serious respiratory infections (like severe pneumonia or bronchitis), comparing standard care to care guided by rapid diagnostic tests and a decision-support tool. **You may be eligible if...** - You are 18 or older with a serious acute respiratory infection - You are being admitted to the hospital - Your doctor does not have concerns about your safety in participating **You may NOT be eligible if...** - You are pregnant, cognitively impaired, a prisoner, or a student or employee of the institution - You have had a cardiac arrest - You are not expected to survive more than 3 days due to a pre-existing illness - You are receiving palliative (comfort-only) care - You are already in another interventional clinical trial Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGPrednisolone 30 mg

This is a glucocorticoid like cortisol used for its anti-inflammatory, immunosuppressive, anti-neoplastic and vasoconstrictive effects. It binds to the glucocorticoid receptor, inhibiting pro-inflammatory signals and promoting anti-inflammatory signals. It has a short duration of action as the half-life is 2.1-3.5 hours and 98% is eliminated in urine. On 21 June 1955 it was granted FDA approval.

DRUGPlacebo

This a tablet identical to prednisolone.


Locations(1)

Queen Mary Hospital

Hong Kong, Hong Kong

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NCT06472219


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