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Effect of displaying nerve block resolution time on postoperative pain complaints

NCT ID NCT07887516

Sponsor: Medical University of South Carolina Source: ClinicalTrials.gov ↗

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
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Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
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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 Results may not be published yet.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)

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Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

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Status unknown
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First seen Oct 21, 2026 · Last updated Oct 22, 2026 · Updated 1 time

Summary

This randomized prospective study will evaluate whether displaying the expected nerve block resolution time on a patient's splint reduces postoperative pain-related complaints after orthopedic surgery. Adults with a fracture who undergo surgery at the Medical University of South Carolina and receive a preoperative nerve block may be eligible. Participants will be randomly assigned to receive standard verbal communication alone or standard verbal communication plus a written display of the expected nerve block resolution time on the splint. The study will compare the number of postoperative pain-related phone calls between the two groups.

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Study facts

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

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 128 people

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

Expected to start

Oct 2026

An estimate. Start dates often move.

Expected to finish

Feb 2027

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.

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 years or older 2. Present with a fracture and will subsequently undergo an operation with the Medical University of South Carolina Department of Orthopaedic Surgery 3. Will receive a preoperative nerve block as part of their standard clinical care Exclusion Criteria: 1. More than one fracture 2. Cognitive impairment or inability to provide informed consent 3. Declines or is unwilling to provide informed consent 4. Currently imprisoned 5. Patients who self-report being pregnant during eligibility screening

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Conditions

The condition(s) this trial relates to.

bone fracture Pain, Postoperative

As listed by the trial registrant

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

Fracture Postoperative pain Rebound pain

How to take part

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  1. The official record

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  2. A doctor treating you

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