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ER study seeks best pain relief for broken bones

NCT ID NCT07314450

Knowledge-focused Sponsor: Region Zealand Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This observational study looks at different ways to manage pain and sedation for adults with broken bones or dislocations in the emergency department. Researchers will compare standard care with various sedation and pain relief methods to see which one patients prefer and which provides the best pain control. About 200 participants will report their pain and satisfaction levels before, during, and after treatment.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 200 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jul 2025

Expected to finish

Jul 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Eligible patients with upper and lower extremity injuries that require painful stabilizing treatment in the emergency department.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. Age ≥18. 2. Patients with the following injuries are eligible: 1. Reduction treatment of shoulder dislocation 2. Reduction treatment of elbow dislocation 3. Reduction treatment of distal radius fractures, application of cast 4. Reduction treatment of finger fractures/dislocation 5. Casting treatment of upper extremity fractures * Proximal humerus fracture, application of fixed sling * Humeral shaft fracture, application of Sarmiento brace * Supracondylar fracture, application of angled cast 6. Reduction treatment of hip dislocation 7. Reduction treatment of patella dislocation 8. Reduction of tibial shaft fracture, application of cast 9. Reduction treatment of ankle fractures including distal tibia fracture 10. Reduction treatment for toe fractures/dislocation 11. Casting treatment of lower extremity fractures * Distal femur fracture, application of cast/traction * Proximal tibia fracture, application of cast or hinged brace * Ankle fracture, application of walker Exclusion Criteria: 1. Unable to give informed consent (e.g. unconscious, psychotic or dementia) 2. Unwilling to participate in the study 3. Prior inclusion in the study 4. Already included in another clinical study at the same day/hospital visit 5. Pregnant or breastfeeding

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Conditions

The condition(s) this trial relates to.

agnosia Arm Injuries Emergencies Leg Injuries pain agnosia Pain, Procedural Patient Satisfaction Personal Satisfaction

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Analgesia Extremity injuries lower Extremity injury Lower extremity fracture Pain, procedural Patient satisfaction Satisfaction Satisfaction, personal Upper extremity fracture Upper extremity injury

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    3 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Emergency Department, Holbæk Hospital

    RECRUITING

    Holbæk, Region Sjælland, 4600, Denmark

  • Emergency Department, Odense University Hospital

    RECRUITING

    Odense, Region Syddanmark, 5000, Denmark

  • Emergency Department, Zealand University Hospital

    RECRUITING

    Køge, Region Sjælland, 4600, Denmark

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