RecruitingACTRN12616000292471

Procedural Sedation in the Emergency Department: Prospective Data Collection

Prospective data collection for procedural sedation performed in the Emergency Department


Sponsor

Dr Adam Michael

Enrollment

20,000 participants

Start Date

Mar 10, 2015

Study Type

Observational

Conditions

Summary

Emergency Department Procedural Sedation is performed many times each day in Emergency Departments around the country. It is becoming an increasingly important skill in the practice of Emergency Medicine. It allows the performance of procedures (including reduction of fractures and dislocations, suturing of wounds, draining of abscesses etc) which in the absence of sedation would be painful and distressing for patients and or technically more difficult or impossible for Doctors. This sedation is increasingly valuable in health systems which demand more efficient use of resources. Effective, safe procedural sedation offers this by saving operating theatres (which are resource intensive) for more complicated procedures. This study aims to add to the current knowledge base by ongoing data collection on procedural sedation done in the Emergency Department. The actual procedural sedation for the patients in the study period will not be influenced by this study. This study will simply document techniques and outcomes of sedation which is done in the normal practice of Emergency Medicine at our Hospital. Complications of the sedation and the procedure will be recorded.


Eligibility

Sex: Both males and femalesMin Age: 6 Monthss

Plain Language Summary

Simplified for easier understanding

This study collects data on how procedural sedation — where patients are given medication to make them drowsy and comfortable during procedures like setting broken bones or draining infections in the emergency department — is performed and how safe it is. The actual care patients receive will not be changed by the study; researchers are simply recording what happens as part of normal emergency department practice. You may be eligible if: - You are 6 months of age or older - You need a procedure in the emergency department that requires sedation - You are able and willing to consent to data collection and follow-up You may NOT be eligible if: - You are unable or unwilling to consent to data collection - A senior clinician is not available in the emergency department to supervise the sedation Talk to your doctor about whether this trial might be 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

Procedural sedation in the ED, All procedures involving sedation which occur in the ED during the study period, will be observed by study staff and complications monitored as they occur. Participants

Procedural sedation in the ED, All procedures involving sedation which occur in the ED during the study period, will be observed by study staff and complications monitored as they occur. Participants will also then be contacted by telephone 1-6 weeks post sedative episode to assess any further complications which occurred following discharge. Patients are observed for the duration of the ED sedative episode, generally 45 minutes or thereabouts, for the recovery period (generally 1 hour), and as well will be followed up by phone between 1 and 6 weeks post discharge from the ED. Patients who are unable to be contacted during this 1-6 week time frame will have phone contact attempts made for up to 3 months. After this point, if still uncontactable, patients willbe deemed lost to follow-up


Locations(2)

Bundaberg Hospital - Bundaberg

QLD, Australia

Mater Adult Hospital - South Brisbane

QLD, Australia

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ACTRN12616000292471