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OpenTrials
Completed

NCT Number: NCT03115684

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

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

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Key information

Age range

16 year and older

Sex eligibility

All sexes

Study type

Observational

Who can participate

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

Inclusion criteria

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

Exclusion criteria

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

Treatment and study plan

Primary outcomes

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

    Time frame: 3 month

Sponsors and collaborators

Lead sponsor

University Hospital, Geneva

Other

Registry information

Official study title

Antalgie à l'Accueil Des Urgences- étude de prévalence

Important dates

Study start
2016
Primary completion
2016
Study completion
2016
First posted
Apr 14, 2017
Registry last updated
Apr 14, 2017

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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