Trial · NCT07886164
Whole-Body Point-of-Care Ultrasound in Older Adults Presenting to the Emergency Department After a Fall
NCT07886164, Recruiting, Kocaeli City Hospital
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Whole-Body Point-of-Care Ultrasound in Older Adults Presenting to the Emergency Department After a Fall. Trials, record NCT07886164. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07886164
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Whole-Body Point-of-Care Ultrasound in Older Adults Presenting to the Emergency Department After a Fall
- NCT number
- NCT07886164
- Status
- Recruiting
- Enrollment
- 105 participants, estimated
- Lead sponsor
- Kocaeli City Hospital
- Conditions
- Accidental Falls, Aged, Syncope
- Interventions
- Whole-body point-of-care ultrasound (POCUS)
- First posted
- 2026-10-21
- Last updated
- 2026-10-21
Source ClinicalTrials.gov
Registered outcomes8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Rate of Change in Emergency Department Management After Whole-Body POCUS | During the emergency department stay (up to 24 hours) | Proportion of patients in whom the treating physician reports at least one change after POCUS in: working diagnosis regarding the cause of the fall, consultation request, additional test request, need for a minor or major procedure, or disposition decision (admission/discharge/transfer), compared with the plan recorded before POCUS. |
| Secondary | Change in Working Diagnosis | During the emergency department stay (up to 24 hours) | Proportion of patients whose working diagnosis regarding the cause of the fall changed after POCUS. |
| Secondary | Change in Consultation Requests | During the emergency department stay (up to 24 hours) | Proportion of patients with a new or cancelled specialist consultation after POCUS. |
| Secondary | Change in Disposition Decision | During the emergency department stay (up to 24 hours) | Proportion of patients whose admission/discharge/transfer decision changed after POCUS. |
| Secondary | Need for Minor or Major Procedures | During the emergency department stay (up to 24 hours) | Proportion of patients in whom a new minor (e.g., arterial blood gas sampling, nasogastric or urinary catheter) or major (e.g., central venous catheter, tube thoracostomy, pericardiocentesis, surgery, procedural sedation) procedure was indicated after POCUS. |
| Secondary | Contribution of POCUS to Identifying the Cause of the Fall | During the emergency department stay (up to 24 hours) | Proportion of patients in whom POCUS identified a pathology considered by the treating physician to be related to the cause of the fall. |
| Secondary | One-Week Mortality | 7 days | All-cause death within 7 days of the index emergency department visit, assessed via the national e-Nabiz health record system or telephone, and its association with POCUS findings. |
| Secondary | Repeat Emergency Department Visits Within One Week | 7 days | Return to the emergency department within 7 days of the index visit, assessed via the national e-Nabiz health record system or telephone, and its association with POCUS findings. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers3
The papers the trial lists on ClinicalTrials.gov.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.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.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07886164
GET https://conductscience.org/api/trials/v1/NCT07886164/registered