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Post-Discharge Pain Management Following Fractures in Adults in the Emergency Department: The POST-PAIN Study

NCT07930897, Recruiting, Odense University Hospital

Trial 8

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

FieldValueSource
TitlePost-Discharge Pain Management Following Fractures in Adults in the Emergency Department: The POST-PAIN StudyClinicalTrials.gov
NCT numberNCT07930897ClinicalTrials.gov
StatusRecruitingClinicalTrials.gov
Enrollment300 participants, estimatedClinicalTrials.gov
Lead sponsorOdense University HospitalClinicalTrials.gov
ConditionsFractures Bone, Acute PainClinicalTrials.gov
First posted2026-11-12ClinicalTrials.gov
Last updated2026-11-12ClinicalTrials.gov

Registered outcomes 12

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescriptionSource
PrimaryProportion of patients with inadequate pain control within 24 hours after dischargeFirst 24 hours after discharge from the emergency department
Inadequate pain control is defined as a maximum patient-reported pain intensity of 4 or above on the numerical rating scale (0-10, where 0 is no pain and 10 is the worst imaginable pain) during the first 24 hours after discharge. It is derived from the worst pain intensity reported in the day 1 entry of the pain diary.
ClinicalTrials.gov
SecondaryMean pain intensity during the 7-day follow-up7 days after dischargeMean of the daily pain intensity reported in the pain diary on the numerical rating scale (0-10).ClinicalTrials.gov
SecondaryNumber of pain-related healthcare contacts7 days after dischargeNumber of contacts with general practitioners, out-of-hours doctors or the emergency department because of pain, reported in the diary and the follow-up interview.ClinicalTrials.gov
SecondaryNumber of patients with sleep disturbance due to pain7 days after dischargeNumber of patients reporting awakenings due to pain in the pain diary.ClinicalTrials.gov
SecondarySleep during the follow-up periodDaily for 7 days after dischargeDaily hours of sleep and sleep compared to normal, reported in the pain diary.ClinicalTrials.gov
SecondaryNumber of patients discharged with a documented post-discharge pain management planDay 0 (at emergency department discharge)Number and proportion of patients with a documented pain management plan in the patient record at discharge.ClinicalTrials.gov
SecondaryNumber and proportion of patients with analgesic side effects7 days after discharge (diary) and at the follow-up interview, 7-14 days after dischargeSide effects reported in the pain diary and the follow-up interview.ClinicalTrials.gov
SecondaryPatient satisfaction with the pain management planAt the follow-up interview, 7-14 days after dischargeRated on a 5-point verbal rating scale: not at all, to a small extent, to some extent, to a high extent, to a very high extent.ClinicalTrials.gov
SecondaryMean pain intensity during the first 24 hours after dischargeFirst 24 hours after dischargeMean pain intensity on the numerical rating scale (0-10) reported in the day 1 pain diary entry.ClinicalTrials.gov
OtherNumber of patients discharged with prescribed opioidsDay 0 (at emergency department discharge)Number and proportion of patients prescribed an opioid analgesic at discharge from the emergency department, based on the patient record and confirmed at the follow-up interview.ClinicalTrials.gov
OtherAnalgesic use7 days after dischargeType, dose and timing of analgesics taken, reported in the pain diary.ClinicalTrials.gov
OtherAmount of unused prescribed analgesics with potential for abuse or dependenceAt the follow-up interview, 7-14 days after dischargeAmount of strongly addictive pain medication (such as opioids) that was prescribed at discharge but remains unused at follow-up, reported by the patient in the follow-up interview.ClinicalTrials.gov

Outcomes 0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured asSource

Results by group 0

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnitsSource

Participant flow 0

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits countedSource

Adverse events 0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEventsSource

Adverse event totals 0

The totals the trial posted for each group.

TotalGroupAffectedAt riskSource

Papers 4

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
15915247BACKGROUNDPubMed
29114833BACKGROUNDPubMed
30681429BACKGROUNDPubMed
36203538BACKGROUNDPubMed

Trial comparisons 0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource

Tests 0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed asSource

Source 4

FieldValueSource
Releasetrials-2026-11-12-0.3.0ClinicalTrials.gov
Release manifest SHA-2564a570df2e7274cee2d4fa2959402fab41880e2cd412e4b590390035fbea69391ClinicalTrials.gov
Registry capture2026-11-12ClinicalTrials.gov
Results copy, AACT2026-03-23ClinicalTrials.gov

The same record as JSON

Release trials-2026-11-12-0.3.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.