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Acute PainNCT03115684

Pain Relief in the Emergency Department Waiting Room: a Prevalence Study

An observational study of Acute Pain, run by University Hospital, Geneva.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Pain in the emergency room is under documented and pain relief suboptimal. Data on nurse driven analgesia in emergency department waiting rooms is lacking. The primary objective of this study is to determine the proportion of patients in pain receiving pain therapy administered by the triage nurse (prevalence study). Read more about this study

Who is it for?
Ages 16 years and older
Conditions the study is for
Acute Pain
How many people
2,371 participants
Where
No sites listed yet
Study dates
1 Mar 2016to 30 May 2016
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 16 years and older
  • All sexes
  • Child, Adult, Older adult

Study population: Patients admited to an emergency department waiting room after triage with a documented pain score upon arrival

Who may be able to join

  • Documented pain score on arrival by the triage nurse and
  • Patients having to wait in the ER waiting room

Who cannot join

  • patients directly admitted to the consultation room
  • patients for whom pain was not recorded

About this study

Official title: Antalgie à l'Accueil Des Urgences- étude de prévalence

Pain in the emergency room is under documented and pain relief suboptimal. Data on nurse driven analgesia in emergency department waiting rooms is lacking. The primary objective of this study is to determine the proportion of patients in pain receiving pain therapy administered by the triage nurse (prevalence study). The secondary objectives are to 1) describe nursing practices in analgesia and adherence to the dedicated protocol; 2) to determine the factors associated with the non administration of painkillers and for these factors, to estimate the strength of the association

Conditions
Acute Pain
Medical subject headings
Acute Pain

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Proportion of patients receiving pain medicine in the ER waiting room by the triage nurse after pain documentation

    Measured: 3 month

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted14 Apr 2017
  2. Study start1 Mar 2016
  3. Primary completion30 May 2016
  4. Study completion30 May 2016

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Prospective
Enrolment
2,371 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03115684
Sponsor's protocol ID
215-00083-(15-272)
Status last verified
Apr 2017
First submitted
11 Apr 2017
Last updated
14 Apr 2017
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Acute Pain, run by University Hospital, Geneva.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 14 Apr 2017. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Proportion of patients receiving pain medicine in the ER waiting room by the triage nurse after pain documentation (time frame: 3 month). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Apr 2017.

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