CompletedNot Applicable

Incidence of Recall After Procedural Sedation With Propofol in the Emergency Department

France248 participantsStarted 2014-07-30

Plain-language summary

The purpose of this study is to determine the incidence of recall in patients managed in emergency department with a procedural sedation protocol using propofol in a population of 250 .

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Adults patients (\> 18 years old) who had a procedural sedation in emergency department using propofol for fracture or joint dislocation reduction * Patients who received an initial injection of Propofol by slow intravenous injection of 1 mg/kg in 20 seconds * Inclusion less than 2 hours from the injection of Propofol * Patients who have signed a consent to participate in the study * Patients covered by social security. Exclusion Criteria: * Patients under 18 years old * Patients who cannot signed the informed consent * Patients who had procedural sedation using other drugs that propofol * Participation in another study type biomedical research

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Recall incidence

Timeframe: At 2 hours (+/- 15 minutes) after procedural sedation with propofol

Trial details

NCT IDNCT02200744

SponsorCentre Hospitalier Universitaire de la Réunion

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2018-09-20

View on ClinicalTrials.gov More Fractures Reduction trials

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.